Antisense modulation of breast cancer-1 expression

ABSTRACT

Antisense compounds, compositions and methods are provided for modulating the expression of breast cancer-1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding breast cancer-1. Methods of using these compounds for modulation of breast cancer-1 expression and for treatment of diseases associated with expression of breast cancer-1 are provided.

FIELD OF THE INVENTION

[0001] The present invention provides compositions and methods for modulating the expression of breast cancer-1. In particular, this invention relates to compounds, particularly oligonucleotides, specifically hybridizable with nucleic acids encoding breast cancer-1. Such compounds have been shown to modulate the expression of breast cancer-1.

BACKGROUND OF THE INVENTION

[0002] Breast cancer affects approximately one in nine women in Western countries. Roughly 90% of breast cancers are sporadic, occurring without germline mutations in known susceptibility loci, but the remaining cases are heritable, caused by mutations of at least two genes, breast cancer-1 and breast cancer-2. Germline mutations of these genes are responsible for approximately two-thirds of all familial breast cancers, and recent genetic epidemiological studies indicate that breast cancer-1 mutation carriers have a lifetime risk of greater than 80% of developing breast cancer. Mutations in breast cancer-1 have been found in approximately 90% of familial breast and ovarian cancers, and, to a lesser extent, males with breast cancer-1 mutations have an increased risk of prostatic cancer (Deng and Brodie, BioEssays, 2000, 22, 728-737; Gao et al., FEBS Lett., 2001, 488, 179-184; Welcsh and King, Hum. Mol. Genet., 2001, 10, 705-713).

[0003] Breast cancer-1 (also known as breast cancer 1, early onset; BRCA-1; BRCA1 ; papillary serous carcinoma of the peritoneum; and PSCP) is considered a tumor suppressor gene because loss of heterozygosity is frequently found in familial cancers, but it has also been described as a caretaker gene, primarily involved in maintaining genome integrity rather than directly inhibiting cell proliferation. Breast cancer-1 interacts with a wide variety of molecules, including tumor suppressors, oncogenes, proteins involved in control of homologous recombination and double-strand break repair in response to DNA damage, cell-cycle regulators, transcriptional co-regulators and chromatin-remodeling proteins, and ubiquitin hydrolases. Thus, breast cancer-1 exerts pleiotropic effects as an important central component in multiple biological pathways that regulate cell-cycle progression, centrosome duplication, genome integrity and DNA damage repair, cell growth and apoptosis, and gene activation and repression (Deng and Brodie, BioEssays, 2000, 22, 728-737; Welcsh and King, Hum. Mol. Genet., 2001, 10, 705-713).

[0004] A region of 11 markers on human chromosome 17q12-q21 very likely to include the gene for breast cancer-1 was identified and the most closely linked marker was characterized (Hall et al., Am. J. Hum. Genet., 1992, 50, 1235-1242). Subsequently, the breast cancer-1 gene was identifed by positional cloning (Miki et al., Science, 1994, 266, 66-71). The murine cDNA homologue of breast cancer-1 was isolated and mapped to mouse chromosome 11, in a region highly syntenic with human chromosome 17q21 (Bennett et al., Genomics, 1995, 29, 576-581; DeGregorio et al., Mamm. Genome, 1996, 7, 242).

[0005] Breast cancer-1 is a nuclear phosphoprotein. Using antibodies, expression and phosphorylation of breast cancer-1 were shown to be cell cycle dependent, with highest levels of expression during replication and mitosis. Breast cancer-1 is phosphorylated and potentially regulated by cyclin-dependent kinases (Chen et al., Cancer Res., 1996, 56, 3168-3172).

[0006] A number of splice variants of breast cancer-1 have been isolated and characterized. Alternative splicing may play a significant role in modulating the subcellular localization of breast cancer-1 (Bachelier et al., Int. J. Cancer, 2000, 88, 519-524), as well as its physiological activity as a growth suppressor and regulator of the expression of the protooncogene c-Fos (Chai et al., Oncogene, 2001, 20, 1357-1367).

[0007] The genomic region containing the breast cancer-1 gene has an unusually high density of repetitive elements which may contribute to chromosomal instability, driving large genomic rearrangements and somatic alterations. Cells that lack breast cancer-1 accumulate chromosomal abnormalities including chromosomal breaks, severe aneuploidy and centrosome amplification, and this chromosomal instability may be the pathogenic basis for breast tumor formation. In one model, cells that have both inherited and somatic inactivating mutations of breast cancer-1 would be unable to repair DNA damage sustained in the following cell cycle and would die, but in rapidly proliferating breast epithelium, some repair-deficient cells may escape death, at least briefly, sustaining damage at many sites, including genes essential to cell cycle checkpoint activation. Mutation of a checkpoint gene would enable a breast cancer-1 null cell to escape death permanently and to proliferate (Welcsh and King, Hum. Mol. Genet., 2001, 10, 705-713).

[0008] One key checkpoint protein is p53, and mice deficient in breast cancer-1 have an increased incidence of alterations in the gene encoding p53. Breast cancer-1 null mouse embryos die late in gestation due to a deficiency in the proliferative burst required for development (Gowen et al., Nat. Genet., 1996, 12, 191-194; Hakem et al., Cell, 1996, 85, 1009-1023). Mutation in either the gene encoding p53 or the gene encoding the G1 cell cycle inhibitor p21 prolonged the survival of breast cancer-1 mutant embryos (Hakem et al., Nat. Genet., 1997, 16, 298-302). Elimination of one allele of the gene encoding p53 in a breast cancer-1 null mouse completely rescues the embryonic lethality of breast cancer-1 deficiency, and restores normal mammary gland development. However, most females develop mammary tumors within 6-12 months. It is believed that widespread apoptosis of the breast cancer-1 null mice is rescued by p53 loss, at the expense of genetic instability. Thus, the breast cancer-1 and p53 genes display a complex pattern of interactions that impact apoptosis, cell cycle control, genomic stability and tumorigenesis (Xu et al., Nat. Genet., 2001, 28, 266-271.).

[0009] Breast cancer-1 also induces apoptosis via a p53-independent pathway. Two types of cell lines, derived from U2OS osteosarcoma cells and MDA435 breast cancer cells, were created for tightly regulateable inducible expression breast cancer-1. Gene expression profiles were examined at various times following breast cancer-1 induction, and apoptosis was found to be triggered through the c-Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) signaling pathway leading to induction of GADD45, the DNA damage-responsive gene (Harkin et al., Cell, 1999, 97, 575-586).

[0010] Breast cancer-1 directly binds DNA without DNA sequence specificity, displaying an preference for branched DNA structures. A large number of molecules of breast cancer-1 bind together in protein-DNA complexes, which form cooperatively between multiple DNA strands. Thus, breast cancer-1 has the characteristics of a protein that is targeted to areas of the genome that are undergoing damage-induced replication and recombinational repair (Paull et al., Proc. Natl. Acad. Sci. U S. A., 2001, 98, 6086-6091).

[0011] Breast cancer-1 also stably interacts with components of DNA repair complexes. Both breast cancer-1 and breast cancer-2 interact with hRAD51, involved in homologous recombination and double-strand break repair, and all three proteins coexist in a biochemical complex that participates homologous recombination during mitosis and meiosis (Chen et al., Mol. Cell., 1998, 2, 317-328).

[0012] Breast cancer-1 is also a component of the RNA polymerase II holoenzyme, acting as a transcriptional coactivator. When a construct expressing the breast cancer-1 gene is transfected into HeLa cells, the breast cancer-1 protein is found associated with the holoenzyme complex, via interaction of its BRCA1 C-terminal (BRCT) domain with the RNA helicase A protein (Anderson et al., Nat. Genet., 1998, 19, 254-256).

[0013] Other proteins interacting with the BRCT domain of breast cancer-1 have been identified, including components of the histone deacetylase complex involved in chromatin remodeling. The BRCT domain of breast cancer-1 interacts in vitro and in vivo with the Rb-binding proteins RbAp46 and RbAp48, with the retinoblastoma (Rb) protein, and with the histone deacetylases HDAC1 and HDAC2 (Yarden and Brody, Proc. Natl. Acad. Sci. USA, 1999, 96, 4983-4988). Furthermore, a breast cancer-1-containing complex with chromatin remodeling activity was isolated from HeLa cells, and a breast cancer-causing deletion in exon 11 of breast cancer-1 completely abolishes p53-mediated stimulation of transcription by breast cancer-1. Thus, a direct role for breast cancer-1 in transcriptional control through modulation of chromatin structure has been established (Bochar et al., Cell, 2000, 102, 257-265).

[0014] A perfect consensus sequence matching a sequence found in granins was identified in the breast cancer-1 protein. Granins are secreted proteins, and their secretion is triggered by cyclic AMP. The expression of some members of the granin family of proteins is regulated by estrogen. The breast cancer-1 protein was shown to localize to the membrane fraction of MDA-MB-468 cells, an invasive breast cancer cell line, suggesting that in these cells, the breast cancer-1 protein is a secreted protein found in the Golgi network and secretory vesicles. Like granins, breast cancer-1 is released upon stimulation by an activator of cyclic AMP, is post-translationally modified, and in induced by estradiol, identifying a previously undescribed mechanism for a tumor suppressor (Jensen et al., Nat. Genet., 1996, 12, 303-308).

[0015] A relationship between papillary serous carcinoma of the peritoneum (PSCP) and ovarian cancer has been observed for years. Reports of women developing peritoneal carcinoma after prophylactic oophorectomy due to a strong history of ovarian carcinoma, as well as reports of peritoneal malignancies in families in which the development of cancer has been associated with breast cancer-1 by linkage analysis, has led to the speculation that peritoneal carcinoma is a part of the familial breast and ovarian cancer syndrome. This has been borne out by the discovery that germline breast cancer-1 mutations were found to occur in PSCP with a frequency comparable to the breast cancer-1 mutation rate in ovarian cancer (Bandera et al., Obstet. Gynecol., 1998, 92, 596-600). Breast cancer-1 related PSCP has a unique pathogenesis in that breast cancer-1 mutation carriers have a higher overall incidence of p53 mutations, and were more likely to exhibit multifocal mutations, but did not exhibit a generalized increase in susceptibility to the acquisition of other somatic mutations (Schorge et al., Cancer Res., 2000, 60, 1361-1364).

[0016] Currently, there are no known therapeutic agents which effectively inhibit the synthesis of breast cancer-1 and to date, investigative strategies aimed at modulating breast cancer-1 function have involved the use of the ligands for the vitamin D receptor and the central (CB1) cannabinoid receptor, retroviral vector therapies, as well as antisense oligonucleotides and antisense expression vectors.

[0017] The ligand for the vitamin D₃ receptor, 1α,25-dihydroxyvitamin D₃ (1α,25(OH)₂D₃) has been found to induce expression of the breast cancer-1 gene. Examination of breast and prostate cancer cell lines revealed that sensitivity to the anti-proliferative effects of 1α,25(OH)₂D₃ were strongly associated with an ability to modulate induction of breast cancer-1. These data suggest the anti-proliferative effects of 1α,25(OH)₂D₃ are mediated, in part, by the up-regulation of breast cancer-1 expression via transcriptional activation by factors induced by the vitamin D receptor and that this growth suppressive pathway is disrupted during the development of breast and prostate cancers (Campbell et al., Oncogene, 2000, 19, 5091-5097).

[0018] Anandamide (N-arachidonoyl-ethanolamine) was the first endogenous brain metabolite shown to act as a ligand of central (CB1) cannabinoid receptors, and a wide range of pharmacological effects have been reported. In addition to inducing hypotension and brachycardia, lowering ocular blood pressure, and affecting lymphocyte and macrophage function, anandamide was shown to potently and selectively inhibit proliferation of the EFM-19 and MCF-7 epitheloid human breast cancer cell lines, perhaps by an indirect mechanism in which prolactin receptor synthesis is suppressed, resulting in the down-regulation of breast cancer-1 (De Petrocellis et al., Proc. Natl. Acad. Sci. U S. A., 1998, 95, 8375-8380) .

[0019] In a model of ovarian cancer, preclinical studies in nude mice xenografts have shown that intrperitoneal injection of retroviral vectors expressing a normal splice variant of breast cancer-1 can inhibit the growth of established intraperitoneal tumors, but attempts to generate an adenoviral vector expressing breast cancer-1 for treatment of this disease have been unsuccessful, despite considerable effort (Tait et al., Hematol. Oncol. Clin. North Am., 1998, 12, 539-552).

[0020] An antisense oligonucleotide, 18 nucleotides in length, targeted to the translation initiation start site of breast cancer-1, as well as an antisense oligonucleotide, 16 nucleotides in length, targeted to the 5′ untranslated region, were used to show that diminished expression of breast cancer-1 increases the proliferative rate of both benign and malignant breast epithelial cells (Thompson et al., Nat. Genet., 1995, 9, 444-450).

[0021] A NIH3T3 mouse fibroblast cell line stably transformed with a vector expressing breast cancer-1 in the antisense orientation showed an accelerated rate of growth, anchorage independent growth and tumorigenicity in nude mice (Rao et al., Oncogene, 1996, 12, 523-528).

[0022] An antisense retroviral construct was introduced into BG-1 estrogen-dependent ovarian adenocarcinoma cells and resulted in reduced breast cancer-1 expression. In contrast to control cells, antisense infected cells demonstrated a growth advantage in monolayer culture in the presence of estrogen and were able to proliferate without estrogen. Reduced levels of breast cancer-1 protein correlated with growth in soft agar and greater tumor formation in nude mice in the absence of estrogen. These data suggest that reduction of breast cancer-1 protein in BG-1 ovarian adenocarcinoma cells may have an effect on cell survival during estrogen deprivation both in vitro and in vivo (Annab et al., Breast Cancer Res., 2000, 2, 139-148).

[0023] Cells exposed to cis-diamminedichloroplatinum(II) (CDDP) undergo cell cycle arrest and subsequently either repair CDDP-induced DNA damage or undergo programmed cell death. In breast and ovarian cancer cell lines resistant to CDDP, a vector expressing the breast cancer-1 cDNA in the antisense direction was used to demonstrate that inhibition of breast cancer-1 gene expression results in an increased sensitivity to CDDP, a decreased proficiency of DNA repair, and an enhanced rate of apoptosis (Husain et al., Cancer Res., 1998, 58, 1120-1123).

[0024] A vector expressing the breast cancer-1 cDNA in the antisense orientation was used to demonstrate that functional inactivation of p53 is a requirement for breast cancer-1-associated tumor development (Reedy et al., Gynecol. Oncol., 2001, 81, 441-446).

[0025] Disclosed and claimed in U.S. Pat. No. 6,130,322 is an isolated polynucleotide comprising the breast cancer-1^((omi2)) sequence or a polynucleotide fully complementary thereto. Antisense is generally disclosed as a means of targeting the control sequences and interfering with production of breast cancer-1 (Murphy et al., 2000).

[0026] Disclosed and claimed in U.S. Pat. Nos. 5,891,857, 6,149,903 and 6,177,410 is a method to reduce the growth of an epithelial ovarian or prostate tumor in a mammal, comprising injecting into the intraperitoneal cavity of said mammal, at the site of said epithelial ovarian or prostate tumor, a vector or a retroviral construct comprising a breast cancer-1 nucleic acid sequence encoding a breast cancer-1 protein having tumor suppressor activity, the nucleic acid sequence operatively linked to a promoter, wherein production of the breast cancer-1 protein results in a decrease in the growth rate of said epithelial ovarian or prostate tumor, and wherein the breast cancer-1 polypeptide is expressed in said epithelial ovarian or prostate tumor at a level and for a period of time sufficient to reduce the growth of said tumor. Antisense inhibition of breast cancer-1 is generally disclosed as a potential means of treating breast or ovarian cancer by accelerating growth of cancer cells and treating with chemotherapeutic drugs (Holt et al., 1999; Holt et al., 2000; Holt et al., 2001).

[0027] Disclosed and claimed in U.S. Pat. Nos. 5,693,473 and 5,747,282 is an isolated DNA coding for a breast cancer-1 polypeptide, said DNA containing regulatory sequences, a replicative cloning vector which comprises said DNA, host cells transformed with an expression system comprising said isolated DNA, a nucleic acid probe specifically hybridizable to a human altered breast cancer-1 DNA, a method of producing breast cancer-1 polypeptide, and a method for screening potential cancer therapeutics. Antisense polynucleotide sequences such as vectors useful in preventing or diminishing the expression of the breast cancer-1 locus polynucleotide are generally disclosed (Shattuck-Eidens et al., 1997; Skolnick et al., 1998).

[0028] Disclosed and claimed in U.S. Pat. Nos. 5,622,829 and 5,821,328 is an isolated nucleic acid comprising a specific breast cancer-1 allele, or a fragment thereof, wherein said fragment is capable of hybridizing with said allele in the presence of wild type breast cancer-1, an isolated polypeptide comprising a C-terminus that is the translation product of a specific allele of breast cancer-1, and a method of screening a patient for a breast, ovarian or prostatic cancer susceptibility. Antisense modulation of gene expression is generally disclosed (King et al., 1998; King et al., 1997).

[0029] Disclosed and claimed in PCT Publication WO 01/02568 is a library of polynucleotides, the library comprising 3351 DNA sequences provided on a nucleic acid array in a computer readable format, corresponding to genes differentially expressed in normal colon tissue relative to colon cancer tissue, wherein one of those sequences is the breast cancer-1 gene. Further claimed is an isolated polynucleotide comprising a nucleotide sequence having at least 90% sequence identity to an identifying sequence of said polynucleotide, a recombinant host cell containing said polynucleotide, an isolated polypeptide encoded by the polynucleotide, and an antibody that specifically binds said polynucleotide. Generally disclosed are ribozymes or antisense oligonucleotides, for use as single stranded DNA probes or as triple-strand forming oligonucleotides to interfere with expression of the corresponding gene (Williams et al., 2001).

[0030] Disclosed and claimed in PCT Publication WO 01/51628 is an isolated nucleic acid molecule selected from a group of novel genes associated with breast cancer, wherein one of those genes is breast cancer-1, comprises a nucleotide sequence which is at least 90% homologous to a nucleotide sequence of Tables 1-6, or is a fragment or a complement thereof, as well as a host cell and a vector containing said sequence, an isolated polypeptide which is encoded by said sequence, an antibody which selectively binds to said polypeptide, and a method for producing or detecting said polypeptide. Further claimed is a method of treating a patient afflicted with breast cancer, the method comprising providing to cells of the patient an antisense oligonucleotide complementary to a polynucleotide corresponding to the breast cancer-1 gene (Lillie et al., 2001).

[0031] Consequently, there remains a long felt need for additional agents capable of effectively inhibiting breast cancer-1 function.

[0032] Antisense technology is emerging as an effective means for reducing the expression of specific gene products and may therefore prove to be uniquely useful in a number of therapeutic, diagnostic, and research applications for the modulation of breast cancer-1 expression.

[0033] The present invention provides compositions and methods for modulating breast cancer-1 expression, including modulation of genomic rearrangements and translocations involving breast cancer-1.

SUMMARY OF THE INVENTION

[0034] The present invention is directed to compounds, particularly antisense oligonucleotides, which are targeted to a nucleic acid encoding breast cancer-1, and which modulate the expression of breast cancer-1. Pharmaceutical and other compositions comprising the compounds of the invention are also provided. Further provided are methods of modulating the expression of breast cancer-1 in cells or tissues comprising contacting said cells or tissues with one or more of the antisense compounds or compositions of the invention. Further provided are methods of treating an animal, particularly a human, suspected of having or being prone to a disease or condition associated with expression of breast cancer-1 by administering a therapeutically or prophylactically effective amount of one or more of the antisense compounds or compositions of the invention.

DETAILED DESCRIPTION OF THE INVENTION

[0035] The present invention employs oligomeric compounds, particularly antisense oligonucleotides, for use in modulating the function of nucleic acid molecules encoding breast cancer-1, ultimately modulating the amount of breast cancer-1 produced. This is accomplished by providing antisense compounds which specifically hybridize with one or more nucleic acids encoding breast cancer-1. As used herein, the terms “target nucleic acid” and “nucleic acid encoding breast cancer-1” encompass DNA encoding breast cancer-1, RNA (including pre-mRNA and mRNA) transcribed from such DNA, and also cDNA derived from such RNA. The specific hybridization of an oligomeric compound with its target nucleic acid interferes with the normal function of the nucleic acid. This modulation of function of a target nucleic acid by compounds which specifically hybridize to it is generally referred to as “antisense”. The functions of DNA to be interfered with include replication and transcription. The functions of RNA to be interfered with include all vital functions such as, for example, translocation of the RNA to the site of protein translation, translocation of the RNA to sites within the cell which are distant from the site of RNA synthesis, translation of protein from the RNA, splicing of the RNA to yield one or more mRNA species, and catalytic activity which may be engaged in or facilitated by the RNA. The overall effect of such interference with target nucleic acid function is modulation of the expression of breast cancer-1. In the context of the present invention, “modulation” means either an increase (stimulation) or a decrease (inhibition) in the expression of a gene. In the context of the present invention, inhibition is the preferred form of modulation of gene expression and mRNA is a preferred target.

[0036] It is preferred to target specific nucleic acids for antisense. “Targeting” an antisense compound to a particular nucleic acid, in the context of this invention, is a multistep process. The process usually begins with the identification of a nucleic acid sequence whose function is to be modulated. This may be, for example, a cellular gene (or mRNA transcribed from the gene) whose expression is associated with a particular disorder or disease state, or a nucleic acid molecule from an infectious agent. In the present invention, the target is a nucleic acid molecule encoding breast cancer-1. The targeting process also includes determination of a site or sites within this gene for the antisense interaction to occur such that the desired effect, e.g., detection or modulation of expression of the protein, will result. Within the context of the present invention, a preferred intragenic site is the region encompassing the translation initiation or termination codon of the open reading frame (ORF) of the gene. Since, as is known in the art, the translation initiation codon is typically 5′-AUG (in transcribed mRNA molecules; 5′-ATG in the corresponding DNA molecule), the translation initiation codon is also referred to as the “AUG codon,” the “start codon” or the “AUG start codon”. A minority of genes have a translation initiation codon having the RNA sequence 5′-GUG, 5′-UUG or 5′-CUG, and 5′-AUA, 5′-ACG and 5′-CUG have been shown to function in vivo. Thus, the terms “translation initiation codon” and “start codon” can encompass many codon sequences, even though the initiator amino acid in each instance is typically methionine (in eukaryotes) or formylmethionine (in prokaryotes). It is also known in the art that eukaryotic and prokaryotic genes may have two or more alternative start codons, any one of which may be preferentially utilized for translation initiation in a particular cell type or tissue, or under a particular set of conditions. In the context of the invention, “start codon” and “translation initiation codon” refer to the codon or codons that are used in vivo to initiate translation of an mRNA molecule transcribed from a gene encoding breast cancer-1, regardless of the sequence(s) of such codons.

[0037] It is also known in the art that a translation termination codon (or “stop codon”) of a gene may have one of three sequences, i.e., 5′-UAA, 5′-UAG and 5′-UGA (the corresponding DNA sequences are 5′-TAA, 5′-TAG and 5′-TGA, respectively). The terms “start codon region” and “translation initiation codon region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5′ or 3′) from a translation initiation codon. Similarly, the terms “stop codon region” and “translation termination codon region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5′ or 3′) from a translation termination codon.

[0038] The open reading frame (ORF) or “coding region,” which is known in the art to refer to the region between the translation initiation codon and the translation termination codon, is also a region which may be targeted effectively. Other target regions include the 5′ untranslated region (5′UTR), known in the art to refer to the portion of an mRNA in the 5′ direction from the translation initiation codon, and thus including nucleotides between the 5′ cap site and the translation initiation codon of an mRNA or corresponding nucleotides on the gene, and the 3′ untranslated region (3′UTR), known in the art to refer to the portion of an mRNA in the 3′ direction from the translation termination codon, and thus including nucleotides between the translation termination codon and 3′ end of an MRNA or corresponding nucleotides on the gene. The 5′ cap of an mRNA comprises an N7-methylated guanosine residue joined to the 5′-most residue of the mRNA via a 5′-5′ triphosphate linkage. The 5′ cap region of an mRNA is considered to include the 5′ cap structure itself as well as the first 50 nucleotides adjacent to the cap. The 5′ cap region may also be a preferred target region.

[0039] Although some eukaryotic mRNA transcripts are directly translated, many contain one or more regions, known as “introns,” which are excised from a transcript before it is translated. The remaining (and therefore translated) regions are known as “exons” and are spliced together to form a continuous mRNA sequence. mRNA splice sites, i.e., intron-exon junctions, may also be preferred target regions, and are particularly useful in situations where aberrant splicing is implicated in disease, or where an overproduction of a particular mRNA splice product is implicated in disease. Aberrant fusion junctions due to rearrangements or deletions are also preferred targets. mRNA transcripts produced via the process of splicing of two (or more) mRNAs from different gene sources are known as “fusion transcripts”. It has also been found that introns can be effective, and therefore preferred, target regions for antisense compounds targeted, for example, to DNA or pre-mRNA.

[0040] It is also known in the art that alternative RNA transcripts can be produced from the same genomic region of DNA. These alternative transcripts are generally known as “variants”. More specifically, “pre-mRNA variants” are transcripts produced from the same genomic DNA that differ from other transcripts produced from the same genomic DNA in either their start or stop position and contain both intronic and extronic regions.

[0041] Upon excision of one or more exon or intron regions or portions thereof during splicing, pre-mRNA variants produce smaller “mRNA variants”. Consequently, mRNA variants are processed pre-mRNA variants and each unique pre-mRNA variant must always produce a unique mRNA variant as a result of splicing. These mRNA variants are also known as “alternative splice variants”. If no splicing of the pre-mRNA variant occurs then the pre-mRNA variant is identical to the mRNA variant.

[0042] It is also known in the art that variants can be produced through the use of alternative signals to start or stop transcription and that pre-mRNAs and mRNAs can possess more that one start codon or stop codon. Variants that originate from a pre-mRNA or mRNA that use alternative start codons are known as “alternative start variants” of that pre-mRNA or mRNA. Those transcripts that use an alternative stop codon are known as “alternative stop variants” of that pre-mRNA or mRNA. One specific type of alternative stop variant is the “polyA variant” in which the multiple transcripts produced result from the alternative selection of one of the “polyA stop signals” by the transcription machinery, thereby producing transcripts that terminate at unique polyA sites.

[0043] Once one or more target sites have been identified, oligonucleotides are chosen which are sufficiently complementary to the target, i.e., hybridize sufficiently well and with sufficient specificity, to give the desired effect.

[0044] In the context of this invention, “hybridization” means hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleoside or nucleotide bases. For example, adenine and thymine are complementary nucleobases which pair through the formation of hydrogen bonds. “Complementary,” as used herein, refers to the capacity for precise pairing between two nucleotides. For example, if a nucleotide at a certain position of an oligonucleotide is capable of hydrogen bonding with a nucleotide at the same position of a DNA or RNA molecule, then the oligonucleotide and the DNA or RNA are considered to be complementary to each other at that position. The oligonucleotide and the DNA or RNA are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleotides which can hydrogen bond with each other. Thus, “specifically hybridizable” and “complementary” are terms which are used to indicate a sufficient degree of complementarity or precise pairing such that stable and specific binding occurs between the oligonucleotide and the DNA or RNA target. It is understood in the art that the sequence of an antisense compound need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable.

[0045] An antisense compound is specifically hybridizable when binding of the compound to the target DNA or RNA molecule interferes with the normal function of the target DNA or RNA to cause a loss of activity, and there is a sufficient degree of complementarity to avoid non-specific binding of the antisense compound to non-target sequences under conditions in which specific binding is desired, i.e., under physiological conditions in the case of in vivo assays or therapeutic treatment, and in the case of in vitro assays, under conditions in which the assays are performed. It is preferred that the antisense compounds of the present invention comprise at least 80% sequence complementarity to a target region within the target nucleic acid, moreover that they comprise 90% sequence complementarity and even more comprise 95% sequence complementarity to the target region within the target nucleic acid sequence to which they are targeted. For example, an antisense compound in which 18 of 20 nucleobases of the antisense compound are complementary, and would therefore specifically hybridize, to a target region would represent 90 percent complementarity. Percent complementarity of an antisense compound with a region of a target nucleic acid can be determined routinely using basic local alignment search tools (BLAST programs) (Altschul et al., J. Mol. Biol., 1990, 215, 403-410; Zhang and Madden, Genome Res., 1997, 7, 649-656).

[0046] Antisense and other compounds of the invention, which hybridize to the target and inhibit expression of the target, are identified through experimentation, and representative sequences of these compounds are hereinbelow identified as preferred embodiments of the invention. The sites to which these preferred antisense compounds are specifically hybridizable are hereinbelow referred to as “preferred target regions” and are therefore preferred sites for targeting. As used herein the term “preferred target region” is defined as at least an 8-nucleobase portion of a target region to which an active antisense compound is targeted. While not wishing to be bound by theory, it is presently believed that these target regions represent regions of the target nucleic acid which are accessible for hybridization.

[0047] While the specific sequences of particular preferred target regions are set forth below, one of skill in the art will recognize that these serve to illustrate and describe particular embodiments within the scope of the present invention. Additional preferred target regions may be identified by one having ordinary skill.

[0048] Target regions 8-80 nucleobases in length comprising a stretch of at least eight (8) consecutive nucleobases selected from within the illustrative preferred target regions are considered to be suitable preferred target regions as well.

[0049] Exemplary good preferred target regions include DNA or RNA sequences that comprise at least the 8 consecutive nucleobases from the 5′-terminus of one of the illustrative preferred target regions (the remaining nucleobases being a consecutive stretch of the same DNA or RNA beginning immediately upstream of the 5′-terminus of the target region and continuing until the DNA or RNA contains about 8 to about 80 nucleobases). Similarly good preferred target regions are represented by DNA or RNA sequences that comprise at least the 8 consecutive nucleobases from the 3′-terminus of one of the illustrative preferred target regions (the remaining nucleobases being a consecutive stretch of the same DNA or RNA,beginning immediately downstream of the 3′-terminus of the target region and continuing until the DNA or RNA contains about 8 to about 80 nucleobases). One having skill in the art, once armed with the empirically-derived preferred target regions illustrated herein will be able, without undue experimentation, to identify further preferred target regions. In addition, one having ordinary skill in the art will also be able to identify additional compounds, including oligonucleotide probes and primers, that specifically hybridize to these preferred target regions using techniques available to the ordinary practitioner in the art.

[0050] Antisense compounds are commonly used as research reagents and diagnostics. For example, antisense oligonucleotides, which are able to inhibit gene expression with exquisite specificity, are often used by those of ordinary skill to elucidate the function of particular genes. Antisense compounds are also used, for example, to distinguish between functions of various members of a biological pathway. Antisense modulation has, therefore, been harnessed for research use.

[0051] For use in kits and diagnostics, the antisense compounds of the present invention, either alone or in combination with other antisense compounds or therapeutics, can be used as tools in differential and/or combinatorial analyses to elucidate expression patterns of a portion or the entire complement of genes expressed within cells and tissues.

[0052] Expression patterns within cells or tissues treated with one or more antisense compounds are compared to control cells or tissues not treated with antisense compounds and the patterns produced are analyzed for differential levels of gene expression as they pertain, for example, to disease association, signaling pathway, cellular localization, expression level, size, structure or function of the genes examined. These analyses can be performed on stimulated or unstimulated cells and in the presence or absence of other compounds which affect expression patterns.

[0053] Examples of methods of gene expression analysis known in the art include DNA arrays or microarrays (Brazma and Vilo, FEBS Lett., 2000, 480, 17-24; Celis, et al., FEBS Lett., 2000, 480, 2-16), SAGE (serial analysis of gene expression)(Madden, et al., Drug Discov. Today, 2000, 5, 415-425), READS (restriction enzyme amplification of digested cDNAs) (Prashar and Weissman, Methods Enzymol., 1999, 303, 258-72), TOGA (total gene expression analysis) (Sutcliffe, et al., Proc. Natl. Acad. Sci. U.S.A., 2000, 97, 1976-81), protein arrays and proteomics (Celis, et al., FEBS Lett., 2000, 480, 2-16; Jungblut, et al., Electrophoresis, 1999, 20, 2100-10), expressed sequence tag (EST) sequencing (Celis, et al., FEBS Lett., 2000, 480, 2-16; Larsson, et al., J. Biotechnol., 2000, 80, 143-57), subtractive RNA fingerprinting (SuRF) (Fuchs, et al., Anal. Biochem., 2000, 286, 91-98; Larson, et al., Cytometry, 2000, 41, 203-208), subtractive cloning, differential display (DD) (Jurecic and Belmont, Curr. Opin. Microbiol., 2000, 3, 316-21), comparative genomic hybridization (Carulli, et al., J. Cell Biochem. Suppl., 1998, 31, 286-96), FISH (fluorescent in situ hybridization) techniques (Going and Gusterson, Eur. J. Cancer, 1999, 35, 1895-904) and mass spectrometry methods (reviewed in To, Comb. Chem. High Throughput Screen, 2000, 3, 235-41).

[0054] The specificity and sensitivity of antisense is also harnessed by those of skill in the art for therapeutic uses. Antisense oligonucleotides have been employed as therapeutic moieties in the treatment of disease states in animals and man. Antisense oligonucleotide drugs, including ribozymes, have been safely and effectively administered to humans and numerous clinical trials are presently underway. It is thus established that oligonucleotides can be useful therapeutic modalities that can be configured to be useful in treatment regimes for treatment of cells, tissues and animals, especially humans.

[0055] In the context of this invention, the term “oligonucleotide” refers to an oligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA) or mimetics thereof. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent internucleoside (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for nucleic acid target and increased stability in the presence of nucleases.

[0056] While antisense oligonucleotides are a preferred form of antisense compound, the present invention comprehends other oligomeric antisense compounds, including but not limited to oligonucleotide mimetics such as are described below. The antisense compounds in accordance with this invention preferably comprise from about 8 to about 80 nucleobases (i.e. from about 8 to about 80 linked nucleosides). Particularly preferred antisense compounds are antisense oligonucleotides from about 8 to about 50 nucleobases, even more preferably those comprising from about 12 to about 30 nucleobases. Antisense compounds include ribozymes, external guide sequence (EGS) oligonucleotides (oligozymes), and other short catalytic RNAs or catalytic oligonucleotides which hybridize to the target nucleic acid and modulate its expression.

[0057] Antisense compounds 8-80 nucleobases in length comprising a stretch of at least eight (8) consecutive nucleobases selected from within the illustrative antisense compounds are considered to be suitable antisense compounds as well.

[0058] Exemplary preferred antisense compounds include DNA or RNA sequences that comprise at least the 8 consecutive nucleobases from the 5′-terminus of one of the illustrative preferred antisense compounds (the remaining nucleobases being a consecutive stretch of the same DNA or RNA beginning immediately upstream of the 5′-terminus of the antisense compound which is specifically hybridizable to the target nucleic acid and continuing until the DNA or RNA contains about 8 to about 80 nucleobases). Similarly preferred antisense compounds are represented by DNA or RNA sequences that comprise at least the 8 consecutive nucleobases from the 3′-terminus of one of the illustrative preferred antisense compounds (the remaining nucleobases being a consecutive stretch of the same DNA or RNA beginning immediately downstream of the 3′-terminus of the antisense compound which is specifically hybridizable to the target nucleic acid and continuing until the DNA or RNA contains about 8 to about 80 nucleobases). One having skill in the art, once armed with the empirically-derived preferred antisense compounds illustrated herein will be able, without undue experimentation, to identify further preferred antisense compounds.

[0059] Antisense and other compounds of the invention, which hybridize to the target and inhibit expression of the target, are identified through experimentation, and representative sequences of these compounds are herein identified as preferred embodiments of the invention. While specific sequences of the antisense compounds are set forth herein, one of skill in the art will recognize that these serve to illustrate and describe particular embodiments within the scope of the present invention. Additional preferred antisense compounds may be identified by one having ordinary skill.

[0060] As is known in the art, a nucleoside is a base-sugar combination. The base portion of the nucleoside is normally a heterocyclic base. The two most common classes of such heterocyclic bases are the purines and the pyrimidines. Nucleotides are nucleosides that further include a phosphate group covalently linked to the sugar portion of the nucleoside. For those nucleosides that include a pentofuranosyl sugar, the phosphate group can be linked to either the 2′, 3′ or 5′ hydroxyl moiety of the sugar. In forming oligonucleotides, the phosphate groups covalently link adjacent nucleosides to one another to form a linear polymeric compound. In turn, the respective ends of this linear polymeric structure can be further joined to form a circular structure, however, open linear structures are generally preferred. In addition, linear structures may also have internal nucleobase complementarity and may therefore fold in a manner as to produce a double stranded structure. Within the oligonucleotide structure, the phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide. The normal linkage or backbone of RNA and DNA is a 3′ to 5′ phosphodiester linkage.

[0061] Specific examples of preferred antisense compounds useful in this invention include oligonucleotides containing modified backbones or non-natural internucleoside linkages. As defined in this specification, oligonucleotides having modified backbones include those that retain a phosphorus atom in the backbone and those that do not have a phosphorus atom in the backbone. For the purposes of this specification, and as sometimes referenced in the art, modified oligonucleotides that do not have a phosphorus atom in their internucleoside backbone can also be considered to be oligonucleosides.

[0062] Preferred modified oligonucleotide backbones include, for example, phosphorothioates, chiral phosphorothioates, phosphorodithioates, phosphotriesters, aminoalkylphosphotri-esters, methyl and other alkyl phosphonates including 3′-alkylene phosphonates, 5′-alkylene phosphonates and chiral phosphonates, phosphinates, phosphoramidates including 3′-amino phosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, selenophosphates and borano-phosphates having normal 3-5′ linkages, 2′-5′ linked analogs of these, and those having inverted polarity wherein one or more internucleotide linkages is a 3′ to 3′, 5′ to 5′ or 2′ to 2′ linkage. Preferred oligonucleotides having inverted polarity comprise a single 3′ to 3′ linkage at the 3′-most internucleotide linkage i.e. a single inverted nucleoside residue which may be abasic (the nucleobase is missing or has a hydroxyl group in place thereof). Various salts, mixed salts and free acid forms are also included.

[0063] Representative United States patents that teach the preparation of the above phosphorus-containing linkages include, but are not limited to, U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,196; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925; 5,519,126; 5,536,821; 5,541,306; 5,550,111; 5,563,253; 5,571,799; 5,587,361; 5,194,599; 5,565,555; 5,527,899; 5,721,218; 5,672,697 and 5,625,050, certain of which are commonly owned with this application, and each of which is herein incorporated by reference.

[0064] Preferred modified oligonucleotide backbones that do not include a phosphorus atom therein have backbones that are formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages. These include those having morpholino linkages (formed in part from the sugar portion of a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfone backbones; formacetyl and thioformacetyl backbones; methylene formacetyl and thioformacetyl backbones; riboacetyl backbones; alkene containing backbones; sulfamate backbones; methyleneimino and methylenehydrazino backbones; sulfonate and sulfonamide backbones; amide backbones; and others having mixed N, O, S and CH₂ component parts.

[0065] Representative United States patents that teach the preparation of the above oligonucleosides include, but are not limited to, U.S. Pat. Nos. 5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033; 5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,610,289; 5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360; 5,677,437; 5,792,608; 5,646,269 and 5,677,439, certain of which are commonly owned with this application, and each of which is herein incorporated by reference.

[0066] In other preferred oligonucleotide mimetics, both the sugar and the internucleoside linkage, i.e., the backbone, of the nucleotide units are replaced with novel groups. The base units are maintained for hybridization with an appropriate nucleic acid target compound. One such oligomeric compound, an oligonucleotide mimetic that has been shown to have excellent hybridization properties, is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar-backbone of an oligonucleotide is replaced with an amide containing backbone, in particular an aminoethylglycine backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of the backbone. Representative United States patents that teach the preparation of PNA compounds include, but are not limited to, U.S. Pat. Nos. 5,539,082; 5,714,331; and 5,719,262, each of which is herein incorporated by reference.

[0067] Further teaching of PNA compounds can be found in Nielsen et al., Science, 1991, 254, 1497-1500.

[0068] Most preferred embodiments of the invention are oligonucleotides with phosphorothioate backbones and oligonucleosides with heteroatom backbones, and in particular —CH₂—NH—O—CH₂—, —CH₂—N(CH₃)—O—CH₂— [known as a methylene (methylimino) or MMI backbone], —CH₂—O—N(CH₃)—CH₂—, —CH₂—N(CH₃)—N(CH₃)—CH₂— and —O—N(CH₃)—CH₂—CH₂— [wherein the native phosphodiester backbone is represented as —O—P—O—CH₂—] of the above referenced U.S. Pat. No. 5,489,677, and the amide backbones of the above referenced U.S. Pat. No. 5,602,240. Also preferred are oligonucleotides having morpholino backbone structures of the above-referenced U.S. Pat. No. 5,034,506.

[0069] Modified oligonucleotides may also contain one or more substituted sugar moieties. Preferred oligonucleotides comprise one of the following at the 2′ position: OH; F; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; O-, S- or N-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl may be substituted or unsubstituted C₁ to C₁₀ alkyl or C₂ to C₁₀ alkenyl and alkynyl. Particularly preferred are O[(CH₂)_(n)O]_(m)CH₃, O(CH₂)_(n)OCH₃, O(CH₂)_(n)NH₂, O(CH₂)_(n)CH₃, O(CH₂)_(n)ONH₂, and O(CH₂)_(n)ON[(CH₂)_(n)CH₃]₂, where n and m are from 1 to about 10. Other preferred oligonucleotides comprise one of the following at the 2′ position: C, to C₁₀ lower alkyl, substituted lower alkyl, alkenyl, alkynyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH₃, OCN, Cl, Br, CN, CF₃, OCF₃, SOCH₃, SO₂CH₃, ONO₂, NO₂, N₃, NH₂, heterocycloalkyl, heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl, an RNA cleaving group, a reporter group, an intercalator, a group for improving the pharmacokinetic properties of an oligonucleotide, or a group for improving the pharmacodynamic properties of an oligonucleotide, and other substituents having similar properties. A preferred modification includes 2′-methoxyethoxy (2′-O—CH₂CH₂OCH₃, also known as 2′-O-(2-methoxyethyl) or 2′-MOE) (Martin et al., Helv. Chim. Acta, 1995, 78, 486-504) i.e., an alkoxyalkoxy group. A further preferred modification includes 2′-dimethylaminooxyethoxy, i.e., a O(CH₂)₂ON(CH₃)₂ group, also known as 2′-DMAOE, as described in examples hereinbelow, and 2′-dimethylaminoethoxyethoxy (also known in the art as 2′-O-dimethyl-amino-ethoxy-ethyl or 2′-DMAEOE), i.e., 2′-O—CH₂—O—CH₂—N(CH₃)₂, also described in examples hereinbelow.

[0070] Other preferred modifications include 2′-methoxy (2′-O—CH₃), 2′-aminopropoxy (2′-OCH₂CH₂CH₂NH₂), 2′-allyl (2′-CH₂—CH═CH₂), 2′-O-allyl (2′-O—CH₂—CH═CH₂) and 2′-fluoro (2′-F). The 2′-modification may be in the arabino (up) position or ribo (down) position. A preferred 2′-arabino modification is 2′-F. Similar modifications may also be made at other positions on the oligonucleotide, particularly the 3′ position of the sugar on the 3′ terminal nucleotide or in 2′-5′ linked oligonucleotides and the 5′ position of 5′ terminal nucleotide. Oligonucleotides may also have sugar mimetics such as cyclobutyl moieties in place of the pentofuranosyl sugar. Representative United States patents that teach the preparation of such modified sugar structures include, but are not limited to, U.S. Pat. Nos. 4,981,957; 5,118,800; 5,319,080; 5,359,044; 5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811; 5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873; 5,646,265; 5,658,873; 5,670,633; 5,792,747; and 5,700,920, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference in its entirety.

[0071] A further preferred modification includes Locked Nucleic Acids (LNAs) in which the 2′-hydroxyl group is linked to the 3′ or 4′ carbon atom of the sugar ring thereby forming a bicyclic sugar moiety. The linkage is preferably a methelyne (—CH₂—)_(n) group bridging the 2′ oxygen atom and the 4′ carbon atom wherein n is 1 or 2. LNAs and preparation thereof are described in WO 98/39352 and WO 99/14226.

[0072] Oligonucleotides may also include nucleobase (often referred to in the art simply as “base”) modifications or substitutions. As used herein, “unmodified” or “natural” nucleobases include the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) and uracil (U). Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl (—C≡C—CH₃) uracil and cytosine and other alkynyl derivatives of pyrimidine bases, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines, 5-halo particularly 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 2-F-adenine, 2-amino-adenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-deazaadenine and 3-deazaguanine and 3-deazaadenine. Further modified nucleobases include tricyclic pyrimidines such as phenoxazine cytidine(1H-pyrimido[5,4-b][1,4]benzoxazin-2(3H)-one), phenothiazine cytidine (1H-pyrimido[5,4-b][1,4]benzothiazin-2(3H)-one), G-clamps such as a substituted phenoxazine cytidine (e.g. 9-(2-aminoethoxy)-H-pyrimido[5,4-b] [1,4]benzoxazin-2(3H)-one), carbazole cytidine (2H-pyrimido[4,5-b]indol-2-one), pyridoindole cytidine (H-pyrido[3′,2′:4,5]pyrrolo[2,3-d]pyrimidin-2-one). Modified nucleobases may also include those in which the purine or pyrimidine base is replaced with other heterocycles, for example 7-deaza-adenine, 7-deazaguanosine, 2-aminopyridine and 2-pyridone. Further nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in The Concise Encyclopedia Of Polymer Science And Engineering, pages 858-859, Kroschwitz, J. I., ed. John Wiley & Sons, 1990, those disclosed by Englisch et al., Angewandte Chemie, International Edition, 1991, 30, 613, and those disclosed by Sanghvi, Y. S., Chapter 15, Antisense Research and Applications, pages 289-302, Crooke, S. T. and Lebleu, B. ed., CRC Press, 1993. Certain of these nucleobases are particularly useful for increasing the binding affinity of the oligomeric compounds of the invention. These include 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and O-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil and 5-propynylcytosine. 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2° C. (Sanghvi, Y. S., Crooke, S. T. and Lebleu, B., eds., Antisense Research and Applications, CRC Press, Boca Raton, 1993, pp. 276-278) and are presently preferred base substitutions, even more particularly when combined with 2′-O-methoxyethyl sugar modifications.

[0073] Representative United States patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include, but are not limited to, the above noted U.S. Pat. Nos. 3,687,808, as well as U.S. Pat. Nos. 4,845,205; 5,130,302; 5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121, 5,596,091; 5,614,617; 5,645,985; 5,830,653; 5,763,588; 6,005,096; and 5,681,941, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference, and U.S. Pat. No. 5,750,692, which is commonly owned with the instant application and also herein incorporated by reference.

[0074] Another modification of the oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more moieties or conjugates which enhance the activity, cellular distribution or cellular uptake of the oligonucleotide. The compounds of the invention can include conjugate groups covalently bound to functional groups such as primary or secondary hydroxyl groups. Conjugate groups of the invention include intercalators, reporter molecules, polyamines, polyamides, polyethylene glycols, polyethers, groups that enhance the pharmacodynamic properties of oligomers, and groups that enhance the pharmacokinetic properties of oligomers. Typical conjugate groups include cholesterols, lipids, phospholipids, biotin, phenazine, folate, phenanthridine, anthraquinone, acridine, fluores-ceins, rhodamines, coumarins, and dyes. Groups that enhance the pharmacodynamic properties, in the context of this invention, include groups that improve oligomer uptake, enhance oligomer resistance to degradation, and/or strengthen sequence-specific hybridization with RNA. Groups that enhance the pharmacokinetic properties, in the context of this invention, include groups that improve oligomer uptake, distribution, metabolism or excretion. Representative conjugate groups are disclosed in International Patent Application PCT/US92/09196, filed Oct. 23, 1992 the entire disclosure of which is incorporated herein by reference. Conjugate moieties include but are not limited to lipid moieties such as a cholesterol moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553-6556), cholic acid (Manoharan et al., Bioorg. Med. Chem. Let., 1994, 4, 1053-1060), a thioether, e.g., hexyl-S-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660, 306-309; Manoharan et al., Bioorg. Med. Chem. Let., 1993, 3, 2765-2770), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20, 533-538), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al., EMBO J., 1991, 10, 1111-1118; Kabanov et al., FEBS Lett., 1990, 259, 327-330; Svinarchuk et al., Biochimie, 1993, 75, 49-54), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethyl-ammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654; Shea et al., Nucl. Acids Res., 1990, 18, 3777-3783), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14, 969-973), or adamantane acetic acid (manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264, 229-237), or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277, 923-937). Oligonucleotides of the invention may also be conjugated to active drug substances, for example, aspirin, warfarin, phenylbutazone, ibuprofen, suprofen, fenbufen, ketoprofen, (S)-(+)-pranoprofen, carprofen, dansylsarcosine, 2,3,5-triiodobenzoic acid, flufenamic acid, folinic acid, a benzothiadiazide, chlorothiazide, a diazepine, indomethicin, a barbiturate, a cephalosporin, a sulfa drug, an antidiabetic, an antibacterial or an antibiotic. Oligonucleotide-drug conjugates and their preparation are described in U.S. patent application Ser. No. 09/334,130 (filed Jun. 15, 1999) which is incorporated herein by reference in its entirety.

[0075] Representative United States patents that teach the preparation of such oligonucleotide conjugates include, but are not limited to, U.S. Pat. Nos. 4,828,979; 4,948,882; 5,218,105; 5,525,465; 5,541,313; 5,545,730; 5,552,538; 5,578,717, 5,580,731; 5,580,731; 5,591,584; 5,109,124; 5,118,802; 5,138,045; 5,414,077; 5,486,603; 5,512,439; 5,578,718; 5,608,046; 4,587,044; 4,605,735; 4,667,025; 4,762,779; 4,789,737; 4,824,941; 4,835,263; 4,876,335; 4,904,582; 4,958,013; 5,082,830; 5,112,963; 5,214,136; 5,082,830; 5,112,963; 5,214,136; 5,245,022; 5,254,469; 5,258,506; 5,262,536; 5,272,250; 5,292,873; 5,317,098; 5,371,241, 5,391,723; 5,416,203, 5,451,463; 5,510,475; 5,512,667; 5,514,785; 5,565,552; 5,567,810; 5,574,142; 5,585,481; 5,587,371; 5,595,726; 5,597,696; 5,599,923; 5,599,928 and 5,688,941, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference.

[0076] It is not necessary for all positions in a given compound to be uniformly modified, and in fact more than one of the aforementioned modifications may be incorporated in a single compound or even at a single nucleoside within an oligonucleotide. The present invention also includes antisense compounds which are chimeric compounds. “Chimeric” antisense compounds or “chimeras,” in the context of this invention, are antisense compounds, particularly oligonucleotides, which contain two or more chemically distinct regions, each made up of at least one monomer unit, i.e., a nucleotide in the case of an oligonucleotide compound. These oligonucleotides typically contain at least one region wherein the oligonucleotide is modified so as to confer upon the oligonucleotide increased resistance to nuclease degradation, increased cellular uptake, increased stability and/or increased binding affinity for the target nucleic acid. An additional region of the oligonucleotide may serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNAse H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of oligonucleotide inhibition of gene expression. The cleavage of RNA:RNA hybrids can, in like fashion, be accomplished through the actions of endoribonucleases, such as interferon-induced RNAseL which cleaves both cellular and viral RNA. Consequently, comparable results can often be obtained with shorter oligonucleotides when chimeric oligonucleotides are used, compared to phosphorothioate deoxyoligonucleotides hybridizing to the same target region. Cleavage of the RNA target can be routinely detected by gel electrophoresis and, if necessary, associated nucleic acid hybridization techniques known in the art.

[0077] Chimeric antisense compounds of the invention may be formed as composite structures of two or more oligonucleotides, modified oligonucleotides, oligonucleosides and/or oligonucleotide mimetics as described above. Such compounds have also been referred to in the art as hybrids or gapmers. Representative United States patents that teach the preparation of such hybrid structures include, but are not limited to, U.S. Pat. Nos. 5,013,830; 5,149,797; 5,220,007; 5,256,775; 5,366,878; 5,403,711; 5,491,133; 5,565,350; 5,623,065; 5,652,355; 5,652,356; and 5,700,922, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference in its entirety.

[0078] The antisense compounds used in accordance with this invention may be conveniently and routinely made through the well-known technique of solid phase synthesis. Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is well known to use similar techniques to prepare oligonucleotides such as the phosphorothioates and alkylated derivatives.

[0079] The compounds of the invention may also be admixed, encapsulated, conjugated or otherwise associated with other molecules, molecule structures or mixtures of compounds, as for example, liposomes, receptor-targeted molecules, oral, rectal, topical or other formulations, for assisting in uptake, distribution and/or absorption. Representative United States patents that teach the preparation of such uptake, distribution and/or absorption-assisting formulations include, but are not limited to, U.S. Pat. Nos. 5,108,921; 5,354,844; 5,416,016; 5,459,127; 5,521,291; 5,543,158; 5,547,932; 5,583,020; 5,591,721; 4,426,330; 4,534,899; 5,013,556; 5,108,921; 5,213,804; 5,227,170; 5,264,221; 5,356,633; 5,395,619; 5,416,016; 5,417,978; 5,462,854; 5,469,854; 5,512,295; 5,527,528; 5,534,259; 5,543,152; 5,556,948; 5,580,575; and 5,595,756, each of which is herein incorporated by reference.

[0080] The antisense compounds of the invention encompass any pharmaceutically acceptable salts, esters, or salts of such esters, or any other compound which, upon administration to an animal, including a human, is capable of providing (directly or indirectly) the biologically active metabolite or residue thereof. Accordingly, for example, the disclosure is also drawn to prodrugs and pharmaceutically acceptable salts of the compounds of the invention, pharmaceutically acceptable salts of such prodrugs, and other bioequivalents.

[0081] The term “prodrug” indicates a therapeutic agent that is prepared in an inactive form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes or other chemicals and/or conditions. In particular, prodrug versions of the oligonucleotides of the invention are prepared as SATE [(S-acetyl-2-thioethyl) phosphate] derivatives according to the methods disclosed in WO 93/24510 to Gosselin et al., published Dec. 9, 1993 or in WO 94/26764 and U.S. Pat. No. 5,770,713 to Imbach et al.

[0082] The term “pharmaceutically acceptable salts” refers to physiologically and pharmaceutically acceptable salts of the compounds of the invention: i.e., salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects thereto.

[0083] Pharmaceutically acceptable base addition salts are formed with metals or amines, such as alkali and alkaline earth metals or organic amines. Examples of metals used as cations are sodium, potassium, magnesium, calcium, and the like. Examples of suitable amines are N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, dicyclohexylamine, ethylenediamine, N-methylglucamine, and procaine (see, for example, Berge et al., “Pharmaceutical Salts,” J. of Pharma Sci., 1977, 66, 1-19). The base addition salts of said acidic compounds are prepared by contacting the free acid form with a sufficient amount of the desired base to produce the salt in the conventional manner. The free acid form may be regenerated by contacting the salt form with an acid and isolating the free acid in the conventional manner. The free acid forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid for purposes of the present invention. As used herein, a “pharmaceutical addition salt” includes a pharmaceutically acceptable salt of an acid form of one of the components of the compositions of the invention. These include organic or inorganic acid salts of the amines. Preferred acid salts are the hydrochlorides, acetates, salicylates, nitrates and phosphates. Other suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of a variety of inorganic and organic acids, such as, for example, with inorganic acids, such as for example hydrochloric acid, hydrobromic acid, sulfuric acid or phosphoric acid; with organic carboxylic, sulfonic, sulfo or phospho acids or N-substituted sulfamic acids, for example acetic acid, propionic acid, glycolic acid, succinic acid, maleic acid, hydroxymaleic acid, methylmaleic acid, fumaric acid, malic acid, tartaric acid, lactic acid, oxalic acid, gluconic acid, glucaric acid, glucuronic acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, salicylic acid, 4-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid, embonic acid, nicotinic acid or isonicotinic acid; and with amino acids, such as the 20 alpha-amino acids involved in the synthesis of proteins in nature, for example glutamic acid or aspartic acid, and also with phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethanesulfonic acid, ethane-1,2-disulfonic acid, benzenesulfonic acid, 4-methylbenzenesulfonic acid, naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, 2- or 3-phosphoglycerate, glucose-6-phosphate, N-cyclohexylsulfamic acid (with the formation of cyclamates), or with other acid organic compounds, such as ascorbic acid. Pharmaceutically acceptable salts of compounds may also be prepared with a pharmaceutically acceptable cation. Suitable pharmaceutically acceptable cations are well known to those skilled in the art and include alkaline, alkaline earth, ammonium and quaternary ammonium cations. Carbonates or hydrogen carbonates are also possible.

[0084] For oligonucleotides, preferred examples of pharmaceutically acceptable salts include but are not limited to (a) salts formed with cations such as sodium, potassium, ammonium, magnesium, calcium, polyamines such as spermine and spermidine, etc.; (b) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; (c) salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, and the like; and (d) salts formed from elemental anions such as chlorine, bromine, and iodine.

[0085] The antisense compounds of the present invention can be utilized for diagnostics, therapeutics, prophylaxis and as research reagents and kits. For therapeutics, an animal, preferably a human, suspected of having a disease or disorder which can be treated by modulating the expression of breast cancer-1 is treated by administering antisense compounds in accordance with this invention. The compounds of the invention can be utilized in pharmaceutical compositions by adding an effective amount of an antisense compound to a suitable pharmaceutically acceptable diluent or carrier. Use of the antisense compounds and methods of the invention may also be useful prophylactically, e.g., to prevent or delay infection, inflammation or tumor formation, for example.

[0086] The antisense compounds of the invention are useful for research and diagnostics, because these compounds hybridize to nucleic acids encoding breast cancer-1, enabling sandwich and other assays to easily be constructed to exploit this fact. Hybridization of the antisense oligonucleotides of the invention with a nucleic acid encoding breast cancer-1 can be detected by means known in the art. Such means may include conjugation of an enzyme to the oligonucleotide, radiolabelling of the oligonucleotide or any other suitable detection means. Kits using such detection means for detecting the level of breast cancer-1 in a sample may also be prepared.

[0087] The present invention also includes pharmaceutical compositions and formulations which include the antisense compounds of the invention. The pharmaceutical compositions of the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic and to mucous membranes including vaginal and rectal delivery), pulmonary, e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Oligonucleotides with at least one 2′-O-methoxyethyl modification are believed to be particularly useful for oral administration.

[0088] Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Coated condoms, gloves and the like may also be useful. Preferred topical formulations include those in which the oligonucleotides of the invention are in admixture with a topical delivery agent such as lipids, liposomes, fatty acids, fatty acid esters, steroids, chelating agents and surfactants. Preferred lipids and liposomes include neutral (e.g. dioleoylphosphatidyl DOPE ethanolamine, dimyristoylphosphatidyl choline DMPC, distearolyphosphatidyl choline) negative (e.g. dimyristoylphosphatidyl glycerol DMPG) and cationic (e.g. dioleoyltetramethylaminopropyl DOTAP and dioleoylphosphatidyl ethanolamine DOTMA). Oligonucleotides of the invention may be encapsulated within liposomes or may form complexes thereto, in particular to cationic liposomes. Alternatively, oligonucleotides may be complexed to lipids, in particular to cationic lipids. Preferred fatty acids and esters include but are not limited arachidonic acid, oleic acid, eicosanoic acid, lauric acid, caprylic acid, capric acid, myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein, dilaurin, glyceryl 1-monocaprate, 1-dodecylazacycloheptan-2-one, an acylcarnitine, an acylcholine, or a C₁₋₁₀ alkyl ester (e.g. isopropylmyristate IPM), monoglyceride, diglyceride or pharmaceutically acceptable salt thereof. Topical formulations are described in detail in U.S. patent application Ser. No. 09/315,298 filed on May 20, 1999 which is incorporated herein by reference in its entirety.

[0089] Compositions and formulations for oral administration include powders or granules, microparticulates, nanoparticulates, suspensions or solutions in water or non-aqueous media, capsules, gel capsules, sachets, tablets or minitablets. Thickeners, flavoring agents, diluents, emulsifiers, dispersing aids or binders may be desirable. Preferred oral formulations are those in which oligonucleotides of the invention are administered in conjunction with one or more penetration enhancers surfactants and chelators. Preferred surfactants include fatty acids and/or esters or salts thereof, bile acids and/or salts thereof. Preferred bile acids/salts include chenodeoxycholic acid (CDCA) and ursodeoxychenodeoxycholic acid (UDCA), cholic acid, dehydrocholic acid, deoxycholic acid, glucholic acid, glycholic acid, glycodeoxycholic acid, taurocholic acid, taurodeoxycholic acid, sodium tauro-24,25-dihydro-fusidate and sodium glycodihydrofusidate. Preferred fatty acids include arachidonic acid, undecanoic acid, oleic acid, lauric acid, caprylic acid, capric acid, myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein, dilaurin, glyceryl 1-monocaprate, 1-dodecylazacycloheptan-2-one, an acylcarnitine, an acylcholine, or a monoglyceride, a diglyceride or a pharmaceutically acceptable salt thereof (e.g. sodium). Also preferred are combinations of penetration enhancers, for example, fatty acids/salts in combination with bile acids/salts. A particularly preferred combination is the sodium salt of lauric acid, capric acid and UDCA. Further penetration enhancers include polyoxyethylene-9-lauryl ether, polyoxyethylene-20-cetyl ether. Oligonucleotides of the invention may be delivered orally, in granular form including sprayed dried particles, or complexed to form micro or nanoparticles. Oligonucleotide complexing agents include poly-amino acids; polyimines; polyacrylates; polyalkylacrylates, polyoxethanes, polyalkylcyanoacrylates; cationized gelatins, albumins, starches, acrylates, polyethyleneglycols (PEG) and starches; polyalkylcyanoacrylates; DEAE-derivatized polyimines, pollulans, celluloses and starches. Particularly preferred complexing agents include chitosan, N-trimethylchitosan, poly-L-lysine, polyhistidine, polyornithine, polyspermines, protamine, polyvinylpyridine, polythiodiethylamino-mathylethylene P(TDAE), polyaminostyrene (e.g. p-amino), poly(methylcyanoacrylate), poly(ethylcyanoacrylate), poly(butylcyanoacrylate), poly(isobutylcyanoacrylate), poly(isohexylcynaoacrylate), DEAE-methacrylate, DEAE-hexylacrylate, DEAE-acrylamide, DEAE-albumin and DEAE-dextran, polymethylacrylate, polyhexylacrylate, poly(D,L-lactic acid), poly(DL-lactic-co-glycolic acid (PLGA), alginate, and polyethyleneglycol (PEG). Oral formulations for oligonucleotides and their preparation are described in detail in U.S. application Ser. Nos. 08/886,829 (filed Jul. 1, 1997), 09/108,673 (filed Jul. 1, 1998), 09/256,515 (filed Feb. 23, 1999), 09/082,624 (filed May 21, 1998) and 09/315,298 (filed May 20, 1999), each of which is incorporated herein by reference in their entirety.

[0090] Compositions and formulations for parenteral, intrathecal or intraventricular administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.

[0091] Pharmaceutical compositions of the present invention include, but are not limited to, solutions, emulsions, and liposome-containing formulations. These compositions may be generated from a variety of components that include, but are not limited to, preformed liquids, self-emulsifying solids and self-emulsifying semisolids.

[0092] The pharmaceutical formulations of the present invention, which may conveniently be presented in unit dosage form, may be prepared according to conventional techniques well known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product.

[0093] The compositions of the present invention may be formulated into any of many possible dosage forms such as, but not limited to, tablets, capsules, gel capsules, liquid syrups, soft gels, suppositories, and enemas. The compositions of the present invention may also be formulated as suspensions in aqueous, non-aqueous or mixed media. Aqueous suspensions may further contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol and/or dextran. The suspension may also contain stabilizers.

[0094] In one embodiment of the present invention the pharmaceutical compositions may be formulated and used as foams. Pharmaceutical foams include formulations such as, but not limited to, emulsions, microemulsions, creams, jellies and liposomes. While basically similar in nature these formulations vary in the components and the consistency of the final product. The preparation of such compositions and formulations is generally known to those skilled in the pharmaceutical and formulation arts and may be applied to the formulation of the compositions of the present invention.

[0095] Emulsions

[0096] The compositions of the present invention may be prepared and formulated as emulsions. Emulsions are typically heterogenous systems of one liquid dispersed in another in the form of droplets usually exceeding 0.1 μm in diameter (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., Volume 1, p. 245; Block in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 2, p. 335; Higuchi et al., in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 301). Emulsions are often biphasic systems comprising two immiscible liquid phases intimately mixed and dispersed with each other. In general, emulsions may be of either the water-in-oil (w/o) or the oil-in-water (o/w) variety. When an aqueous phase is finely divided into and dispersed as minute droplets into a bulk oily phase, the resulting composition is called a water-in-oil (w/o) emulsion. Alternatively, when an oily phase is finely divided into and dispersed as minute droplets into a bulk aqueous phase, the resulting composition is called an oil-in-water (o/w) emulsion. Emulsions may contain additional components in addition to the dispersed phases, and the active drug which may be present as a solution in either the aqueous phase, oily phase or itself as a separate phase. Pharmaceutical excipients such as emulsifiers, stabilizers, dyes, and anti-oxidants may also be present in emulsions as needed. Pharmaceutical emulsions may also be multiple emulsions that are comprised of more than two phases such as, for example, in the case of oil-in-water-in-oil (o/w/o) and water-in-oil-in-water (w/o/w) emulsions. Such complex formulations often provide certain advantages that simple binary emulsions do not. Multiple emulsions in which individual oil droplets of an o/w emulsion enclose small water droplets constitute a w/o/w emulsion. Likewise a system of oil droplets enclosed in globules of water stabilized in an oily continuous phase provides an o/w/o emulsion.

[0097] Emulsions are characterized by little or no thermodynamic stability. Often, the dispersed or discontinuous phase of the emulsion is well dispersed into the external or continuous phase and maintained in this form through the means of emulsifiers or the viscosity of the formulation. Either of the phases of the emulsion may be a semisolid or a solid, as is the case of emulsion-style ointment bases and creams. Other means of stabilizing emulsions entail the use of emulsifiers that may be incorporated into either phase of the emulsion. Emulsifiers may broadly be classified into four categories: synthetic surfactants, naturally occurring emulsifiers, absorption bases, and finely dispersed solids (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

[0098] Synthetic surfactants, also known as surface active agents, have found wide applicability in the formulation of emulsions and have been reviewed in the literature (Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), Marcel Dekker, Inc., New York, N.Y., 1988, volume 1, p. 199). Surfactants are typically amphiphilic and comprise a hydrophilic and a hydrophobic portion. The ratio of the hydrophilic to the hydrophobic nature of the surfactant has been termed the hydrophile/lipophile balance (HLB) and is a valuable tool in categorizing and selecting surfactants in the preparation of formulations. Surfactants may be classified into different classes based on the nature of the hydrophilic group: nonionic, anionic, cationic and amphoteric (Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285).

[0099] Naturally occurring emulsifiers used in emulsion formulations include lanolin, beeswax, phosphatides, lecithin and acacia. Absorption bases possess hydrophilic properties such that they can soak up water to form w/o emulsions yet retain their semisolid consistencies, such as anhydrous lanolin and hydrophilic petrolatum. Finely divided solids have also been used as good emulsifiers especially in combination with surfactants and in viscous preparations. These include polar inorganic solids, such as heavy metal hydroxides, nonswelling clays such as bentonite, attapulgite, hectorite, kaolin, montmorillonite, colloidal aluminum silicate and colloidal magnesium aluminum silicate, pigments and nonpolar solids such as carbon or glyceryl tristearate.

[0100] A large variety of non-emulsifying materials are also included in emulsion formulations and contribute to the properties of emulsions. These include fats, oils, waxes, fatty acids, fatty alcohols, fatty esters, humectants, hydrophilic colloids, preservatives and antioxidants (Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

[0101] Hydrophilic colloids or hydrocolloids include naturally occurring gums and synthetic polymers such as polysaccharides (for example, acacia, agar, alginic acid, carrageenan, guar gum, karaya gum, and tragacanth), cellulose derivatives (for example, carboxymethylcellulose and carboxypropylcellulose), and synthetic polymers (for example, carbomers, cellulose ethers, and carboxyvinyl polymers). These disperse or swell in water to form colloidal solutions that stabilize emulsions by forming strong interfacial films around the dispersed-phase droplets and by increasing the viscosity of the external phase.

[0102] Since emulsions often contain a number of ingredients such as carbohydrates, proteins, sterols and phosphatides that may readily support the growth of microbes, these formulations often incorporate preservatives. Commonly used preservatives included in emulsion formulations include methyl paraben, propyl paraben, quaternary ammonium salts, benzalkonium chloride, esters of p-hydroxybenzoic acid, and boric acid. Antioxidants are also commonly added to emulsion formulations to prevent deterioration of the formulation. Antioxidants used may be free radical scavengers such as tocopherols, alkyl gallates, butylated hydroxyanisole, butylated hydroxytoluene, or reducing agents such as ascorbic acid and sodium metabisulfite, and antioxidant synergists such as citric acid, tartaric acid, and lecithin.

[0103] The application of emulsion formulations via dermatological, oral and parenteral routes and methods for their manufacture have been reviewed in the literature (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Emulsion formulations for oral delivery have been very widely used because of ease of formulation, as well as efficacy from an absorption and bioavailability standpoint (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Mineral-oil base laxatives, oil-soluble vitamins and high fat nutritive preparations are among the materials that have commonly been administered orally as o/w emulsions.

[0104] In one embodiment of the present invention, the compositions of oligonucleotides and nucleic acids are formulated as microemulsions. A microemulsion may be defined as a system of water, oil and amphiphile which is a single optically isotropic and thermodynamically stable liquid solution (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245). Typically microemulsions are systems that are prepared by first dispersing an oil in an aqueous surfactant solution and then adding a sufficient amount of a fourth component, generally an intermediate chain-length alcohol to form a transparent system. Therefore, microemulsions have also been described as thermodynamically stable, isotropically clear dispersions of two immiscible liquids that are stabilized by interfacial films of surface-active molecules (Leung and Shah, in: Controlled Release of Drugs: Polymers and Aggregate Systems, Rosoff, M., Ed., 1989, VCH Publishers, New York, pages 185-215). Microemulsions commonly are prepared via a combination of three to five components that include oil, water, surfactant, cosurfactant and electrolyte. Whether the microemulsion is of the water-in-oil (w/o) or an oil-in-water (o/w) type is dependent on the properties of the oil and surfactant used and on the structure and geometric packing of the polar heads and hydrocarbon tails of the surfactant molecules (Schott, in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 271).

[0105] The phenomenological approach utilizing phase diagrams has been extensively studied and has yielded a comprehensive knowledge, to one skilled in the art, of how to formulate microemulsions (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335). Compared to conventional emulsions, microemulsions offer the advantage of solubilizing water-insoluble drugs in a formulation of thermodynamically stable droplets that are formed spontaneously.

[0106] Surfactants used in the preparation of microemulsions include, but are not limited to, ionic surfactants, non-ionic surfactants, Brij 96, polyoxyethylene oleyl ethers, polyglycerol fatty acid esters, tetraglycerol monolaurate (ML310), tetraglycerol monooleate (MO310), hexaglycerol monooleate (PO310), hexaglycerol pentaoleate (PO500), decaglycerol monocaprate (MCA750), decaglycerol monooleate (MO750), decaglycerol sequioleate (SO750), decaglycerol decaoleate (DAO750), alone or in combination with cosurfactants. The cosurfactant, usually a short-chain alcohol such as ethanol, 1-propanol, and 1-butanol, serves to increase the interfacial fluidity by penetrating into the surfactant film and consequently creating a disordered film because of the void space generated among surfactant molecules. Microemulsions may, however, be prepared without the use of cosurfactants and alcohol-free self-emulsifying microemulsion systems are known in the art. The aqueous phase may typically be, but is not limited to, water, an aqueous solution of the drug, glycerol, PEG300, PEG400, polyglycerols, propylene glycols, and derivatives of ethylene glycol. The oil phase may include, but is not limited to, materials such as Captex 300, Captex 355, Capmul MCM, fatty acid esters, medium chain (C8-C12) mono, di, and tri-glycerides, polyoxyethylated glyceryl fatty acid esters, fatty alcohols, polyglycolized glycerides, saturated polyglycolized C8-C10 glycerides, vegetable oils and silicone oil.

[0107] Microemulsions are particularly of interest from the standpoint of drug solubilization and the enhanced absorption of drugs. Lipid based microemulsions (both o/w and w/o) have been proposed to enhance the oral bioavailability of drugs, including peptides (Constantinides et al., Pharmaceutical Research, 1994, 11, 1385-1390; Ritschel, Meth. Find. Exp. Clin. Pharmacol., 1993, 13, 205). Microemulsions afford advantages of improved drug solubilization, protection of drug from enzymatic hydrolysis, possible enhancement of drug absorption due to surfactant-induced alterations in membrane fluidity and permeability, ease of preparation, ease of oral administration over solid dosage forms, improved clinical potency, and decreased toxicity (Constantinides et al., Pharmaceutical Research, 1994, 11, 1385; Ho et al., J. Pharm. Sci., 1996, 85, 138-143). Often microemulsions may form spontaneously when their components are brought together at ambient temperature. This may be particularly advantageous when formulating thermolabile drugs, peptides or oligonucleotides. Microemulsions have also been effective in the transdermal delivery of active components in both cosmetic and pharmaceutical applications. It is expected that the microemulsion compositions and formulations of the present invention will facilitate the increased systemic absorption of oligonucleotides and nucleic acids from the gastrointestinal tract, as well as improve the local cellular uptake of oligonucleotides and nucleic acids within the gastrointestinal tract, vagina, buccal cavity and other areas of administration.

[0108] Microemulsions of the present invention may also contain additional components and additives such as sorbitan monostearate (Grill 3), Labrasol, and penetration enhancers to improve the properties of the formulation and to enhance the absorption of the oligonucleotides and nucleic acids of the present invention. Penetration enhancers used in the microemulsions of the present invention may be classified as belonging to one of five broad categories—surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92). Each of these classes has been discussed above.

[0109] Liposomes

[0110] There are many organized surfactant structures besides microemulsions that have been studied and used for the formulation of drugs. These include monolayers, micelles, bilayers and vesicles. Vesicles, such as liposomes, have attracted great interest because of their specificity and the duration of action they offer from the standpoint of drug delivery. As used in the present invention, the term “liposome” means a vesicle composed of amphiphilic lipids arranged in a spherical bilayer or bilayers.

[0111] Liposomes are unilamellar or multilamellar vesicles which have a membrane formed from a lipophilic material and an aqueous interior. The aqueous portion contains the composition to be delivered. Cationic liposomes possess the advantage of being able to fuse to the cell wall. Non-cationic liposomes, although not able to fuse as efficiently with the cell wall, are taken up by macrophages in vivo.

[0112] In order to cross intact mammalian skin, lipid vesicles must pass through a series of fine pores, each with a diameter less than 50 nm, under the influence of a suitable transdermal gradient. Therefore, it is desirable to use a liposome which is highly deformable and able to pass through such fine pores.

[0113] Further advantages of liposomes include; liposomes obtained from natural phospholipids are biocompatible and biodegradable; liposomes can incorporate a wide range of water and lipid soluble drugs; liposomes can protect encapsulated drugs in their internal compartments from metabolism and degradation (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245). Important considerations in the preparation of liposome formulations are the lipid surface charge, vesicle size and the aqueous volume of the liposomes.

[0114] Liposomes are useful for the transfer and delivery of active ingredients to the site of action. Because the liposomal membrane is structurally similar to biological membranes, when liposomes are applied to a tissue, the liposomes start to merge with the cellular membranes and as the merging of the liposome and cell progresses, the liposomal contents are emptied into the cell where the active agent may act.

[0115] Liposomal formulations have been the focus of extensive investigation as the mode of delivery for many drugs. There is growing evidence that for topical administration, liposomes present several advantages over other formulations. Such advantages include reduced side-effects related to high systemic absorption of the administered drug, increased accumulation of the administered drug at the desired target, and the ability to administer a wide variety of drugs, both hydrophilic and hydrophobic, into the skin.

[0116] Several reports have detailed the ability of liposomes to deliver agents including high-molecular weight DNA into the skin. Compounds including analgesics, antibodies, hormones and high-molecular weight DNAs have been administered to the skin. The majority of applications resulted in the targeting of the upper epidermis.

[0117] Liposomes fall into two broad classes. Cationic liposomes are positively charged liposomes which interact with the negatively charged DNA molecules to form a stable complex. The positively charged DNA/liposome complex binds to the negatively charged cell surface and is internalized in an endosome. Due to the acidic pH within the endosome, the liposomes are ruptured, releasing their contents into the cell cytoplasm (Wang et al., Biochem. Biophys. Res. Commun., 1987, 147, 980-985).

[0118] Liposomes which are pH-sensitive or negatively-charged, entrap DNA rather than complex with it. Since both the DNA and the lipid are similarly charged, repulsion rather than complex formation occurs. Nevertheless, some DNA is entrapped within the aqueous interior of these liposomes. pH-sensitive liposomes have been used to deliver DNA encoding the thymidine kinase gene to cell monolayers in culture. Expression of the exogenous gene was detected in the target cells (Zhou et al., Journal of Controlled Release, 1992, 19, 269-274).

[0119] One major type of liposomal composition includes phospholipids other than naturally-derived phosphatidylcholine. Neutral liposome compositions, for example, can be formed from dimyristoyl phosphatidylcholine (DMPC) or dipalmitoyl phosphatidylcholine (DPPC). Anionic liposome compositions generally are formed from dimyristoyl phosphatidylglycerol, while anionic fusogenic liposomes are formed primarily from dioleoyl phosphatidylethanolamine (DOPE). Another type of liposomal composition is formed from phosphatidylcholine (PC) such as, for example, soybean PC, and egg PC. Another type is formed from mixtures of phospholipid and/or phosphatidylcholine and/or cholesterol.

[0120] Several studies have assessed the topical delivery of liposomal drug formulations to the skin. Application of liposomes containing interferon to guinea pig skin resulted in a reduction of skin herpes sores while delivery of interferon via other means (e.g. as a solution or as an emulsion) were ineffective (Weiner et al., Journal of Drug Targeting, 1992, 2, 405-410). Further, an additional study tested the efficacy of interferon administered as part of a liposomal formulation to the administration of interferon using an aqueous system, and concluded that the liposomal formulation was superior to aqueous administration (du Plessis et al., Antiviral Research, 1992, 18, 259-265).

[0121] Non-ionic liposomal systems have also been examined to determine their utility in the delivery of drugs to the skin, in particular systems comprising non-ionic surfactant and cholesterol. Non-ionic liposomal formulations comprising Novasome™ I (glyceryl dilaurate/cholesterol/polyoxyethylene-10-stearyl ether) and Novasome™ II (glyceryl distearate/cholesterol/polyoxyethylene-10-stearyl ether) were used to deliver cyclosporin-A into the dermis of mouse skin. Results indicated that such non-ionic liposomal systems were effective in facilitating the deposition of cyclosporin-A into different layers of the skin (Hu et al. S.T.P. Pharma. Sci., 1994, 4, 6, 466).

[0122] Liposomes also include “sterically stabilized” liposomes, a term which, as used herein, refers to liposomes comprising one or more specialized lipids that, when incorporated into liposomes, result in enhanced circulation lifetimes relative to liposomes lacking such specialized lipids. Examples of sterically stabilized liposomes are those in which part of the vesicle-forming lipid portion of the liposome (A) comprises one or more glycolipids, such as monosialoganglioside G_(M1), or (B) is derivatized with one or more hydrophilic polymers, such as a polyethylene glycol (PEG) moiety. While not wishing to be bound by any particular theory, it is thought in the art that, at least for sterically stabilized liposomes containing gangliosides, sphingomyelin, or PEG-derivatized lipids, the enhanced circulation half-life of these sterically stabilized liposomes derives from a reduced uptake into cells of the reticuloendothelial system (RES) (Allen et al., FEBS Letters, 1987, 223, 42; Wu et al., Cancer Research, 1993, 53, 3765).

[0123] Various liposomes comprising one or more glycolipids are known in the art. Papahadjopoulos et al. (Ann. N.Y. Acad. Sci., 1987, 507, 64) reported the ability of monosialoganglioside G_(M1), galactocerebroside sulfate and phosphatidylinositol to improve blood half-lives of liposomes. These findings were expounded upon by Gabizon et al. (Proc. Natl. Acad. Sci. U.S.A., 1988, 85, 6949). U.S. Pat. No. 4,837,028 and WO 88/04924, both to Allen et al., disclose liposomes comprising (1) sphingomyelin and (2) the ganglioside G_(M1) or a galactocerebroside sulfate ester. U.S. Pat. No. 5,543,152 (Webb et al.) discloses liposomes comprising sphingomyelin. Liposomes comprising 1,2-sn-dimyristoylphosphatidylcholine are disclosed in WO 97/13499 (Lim et al.).

[0124] Many liposomes comprising lipids derivatized with one or more hydrophilic polymers, and methods of preparation thereof, are known in the art. Sunamoto et al. (Bull. Chem. Soc. Jpn., 1980, 53, 2778) described liposomes comprising a nonionic detergent, 2C₁₂15G, that contains a PEG moiety. Illum et al. (FEBS Lett., 1984, 167, 79) noted that hydrophilic coating of polystyrene particles with polymeric glycols results in significantly enhanced blood half-lives. Synthetic phospholipids modified by the attachment of carboxylic groups of polyalkylene glycols (e.g., PEG) are described by Sears (U.S. Pat. Nos. 4,426,330 and 4,534,899). Klibanov et al. (FEBS Lett., 1990, 268, 235) described experiments demonstrating that liposomes comprising phosphatidylethanolamine (PE) derivatized with PEG or PEG stearate have significant increases in blood circulation half-lives. Blume et al. (Biochimica et Biophysica Acta, 1990, 1029, 91) extended such observations to other PEG-derivatized phospholipids, e.g., DSPE-PEG, formed from the combination of distearoylphosphatidylethanolamine (DSPE) and PEG. Liposomes having covalently bound PEG moieties on their external surface are described in European Patent No. EP 0 445 131 B1 and WO 90/04384 to Fisher. Liposome compositions containing 1-20 mole percent of PE derivatized with PEG, and methods of use thereof, are described by Woodle et al. (U.S. Pat. Nos. 5,013,556 and 5,356,633) and Martin et al. (U.S. Pat. No. 5,213,804 and European Patent No. EP 0 496 813 B1). Liposomes comprising a number of other lipid-polymer conjugates are disclosed in WO 91/05545 and U.S. Pat. No. 5,225,212 (both to Martin et al.) and in WO 94/20073 (Zalipsky et al.) Liposomes comprising PEG-modified ceramide lipids are described in WO 96/10391 (Choi et al.). U.S. Pat. Nos. 5,540,935 (Miyazaki et al.) and 5,556,948 (Tagawa et al.) describe PEG-containing liposomes that can be further derivatized with functional moieties on their surfaces.

[0125] A limited number of liposomes comprising nucleic acids are known in the art. WO 96/40062 to Thierry et al. discloses methods for encapsulating high molecular weight nucleic acids in liposomes. U.S. Pat. No. 5,264,221 to Tagawa et al. discloses protein-bonded liposomes and asserts that the contents of such liposomes may include an antisense RNA. U.S. Pat. No. 5,665,710 to Rahman et al. describes certain methods of encapsulating oligodeoxynucleotides in liposomes. WO 97/04787 to Love et al. discloses liposomes comprising antisense oligonucleotides targeted to the raf gene.

[0126] Transfersomes are yet another type of liposomes, and are highly deformable lipid aggregates which are attractive candidates for drug delivery vehicles. Transfersomes may be described as lipid droplets which are so highly deformable that they are easily able to penetrate through pores which are smaller than the droplet. Transfersomes are adaptable to the environment in which they are used, e.g. they are self-optimizing (adaptive to the shape of pores in the skin), self-repairing, frequently reach their targets without fragmenting, and often self-loading. To make transfersomes it is possible to add surface edge-activators, usually surfactants, to a standard liposomal composition. Transfersomes have been used to deliver serum albumin to the skin. The transfersome-mediated delivery of serum albumin has been shown to be as effective as subcutaneous injection of a solution containing serum albumin.

[0127] Surfactants find wide application in formulations such as emulsions (including microemulsions) and liposomes. The most common way of classifying and ranking the properties of the many different types of surfactants, both natural and synthetic, is by the use of the hydrophile/lipophile balance (HLB). The nature of the hydrophilic group (also known as the “head”) provides the most useful means for categorizing the different surfactants used in formulations (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, NY, 1988, p. 285).

[0128] If the surfactant molecule is not ionized, it is classified as a nonionic surfactant. Nonionic surfactants find wide application in pharmaceutical and cosmetic products and are usable over a wide range of pH values. In general their HLB values range from 2 to about 18 depending on their structure. Nonionic surfactants include nonionic esters such as ethylene glycol esters, propylene glycol esters, glyceryl esters, polyglyceryl esters, sorbitan esters, sucrose esters, and ethoxylated esters. Nonionic alkanolamides and ethers such as fatty alcohol ethoxylates, propoxylated alcohols, and ethoxylated/propoxylated block polymers are also included in this class. The polyoxyethylene surfactants are the most popular members of the nonionic surfactant class.

[0129] If the surfactant molecule carries a negative charge when it is dissolved or dispersed in water, the surfactant is classified as anionic. Anionic surfactants include carboxylates such as soaps, acyl lactylates, acyl amides of amino acids, esters of sulfuric acid such as alkyl sulfates and ethoxylated alkyl sulfates, sulfonates such as alkyl benzene sulfonates, acyl isethionates, acyl taurates and sulfosuccinates, and phosphates. The most important members of the anionic surfactant class are the alkyl sulfates and the soaps.

[0130] If the surfactant molecule carries a positive charge when it is dissolved or dispersed in water, the surfactant is classified as cationic. Cationic surfactants include quaternary ammonium salts and ethoxylated amines. The quaternary ammonium salts are the most used members of this class.

[0131] If the surfactant molecule has the ability to carry either a positive or negative charge, the surfactant is classified as amphoteric. Amphoteric surfactants include acrylic acid derivatives, substituted alkylamides, N-alkylbetaines and phosphatides.

[0132] The use of surfactants in drug products, formulations and in emulsions has been reviewed (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988, p. 285).

[0133] Penetration Enhancers

[0134] In one embodiment, the present invention employs various penetration enhancers to effect the efficient delivery of nucleic acids, particularly oligonucleotides, to the skin of animals. Most drugs are present in solution in both ionized and nonionized forms. However, usually only lipid soluble or lipophilic drugs readily cross cell membranes. It has been discovered that even non-lipophilic drugs may cross cell membranes if the membrane to be crossed is treated with a penetration enhancer. In addition to aiding the diffusion of non-lipophilic drugs across cell membranes, penetration enhancers also enhance the permeability of lipophilic drugs.

[0135] Penetration enhancers may be classified as belonging to one of five broad categories, i.e., surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p.92). Each of the above mentioned classes of penetration enhancers are described below in greater detail.

[0136] Surfactants: In connection with the present invention, surfactants (or “surface-active agents”) are chemical entities which, when dissolved in an aqueous solution, reduce the surface tension of the solution or the interfacial tension between the aqueous solution and another liquid, with the result that absorption of oligonucleotides through the mucosa is enhanced. In addition to bile salts and fatty acids, these penetration enhancers include, for example, sodium lauryl sulfate, polyoxyethylene-9-lauryl ether and polyoxyethylene-20-cetyl ether) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p.92); and perfluorochemical emulsions, such as FC-43. Takahashi et al., J. Pharm. Pharmacol., 1988, 40, 252).

[0137] Fatty acids: Various fatty acids and their derivatives which act as penetration enhancers include, for example, oleic acid, lauric acid, capric acid (n-decanoic acid), myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein (1-monooleoyl-rac-glycerol), dilaurin, caprylic acid, arachidonic acid, glycerol 1-monocaprate, 1-dodecylazacycloheptan-2-one, acylcarnitines, acylcholines, C₁₋₁₀ alkyl esters thereof (e.g., methyl, isopropyl and t-butyl), and mono- and di-glycerides thereof (i.e., oleate, laurate, caprate, myristate, palmitate, stearate, linoleate, etc.) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p.92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; El Hariri et al., J. Pharm. Pharmacol., 1992, 44, 651-654).

[0138] Bile salts: The physiological role of bile includes the facilitation of dispersion and absorption of lipids and fat-soluble vitamins (Brunton, Chapter 38 in: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman et al. Eds., McGraw-Hill, New York, 1996, pp. 934-935). Various natural bile salts, and their synthetic derivatives, act as penetration enhancers. Thus the term “bile salts” includes any of the naturally occurring components of bile as well as any of their synthetic derivatives. The bile salts of the invention include, for example, cholic acid (or its pharmaceutically acceptable sodium salt, sodium cholate), dehydrocholic acid (sodium dehydrocholate), deoxycholic acid (sodium deoxycholate), glucholic acid (sodium glucholate), glycholic acid (sodium glycocholate), glycodeoxycholic acid (sodium glycodeoxycholate), taurocholic acid (sodium taurocholate), taurodeoxycholic acid (sodium taurodeoxycholate), chenodeoxycholic acid (sodium chenodeoxycholate), ursodeoxycholic acid (UDCA), sodium tauro-24,25-dihydro-fusidate (STDHF), sodium glycodihydrofusidate and polyoxyethylene-9-lauryl ether (POE) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Swinyard, Chapter 39 In: Remington's Pharmaceutical Sciences, 18th Ed., Gennaro, ed., Mack Publishing Co., Easton, Pa., 1990, pages 782-783; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Yamamoto et al., J. Pharm. Exp. Ther., 1992, 263, 25; Yamashita et al., J. Pharm. Sci., 1990, 79, 579-583).

[0139] Chelating Agents: Chelating agents, as used in connection with the present invention, can be defined as compounds that remove metallic ions from solution by forming complexes therewith, with the result that absorption of oligonucleotides through the mucosa is enhanced. With regards to their use as penetration enhancers in the present invention, chelating agents have the added advantage of also serving as DNase inhibitors, as most characterized DNA nucleases require a divalent metal ion for catalysis and are thus inhibited by chelating agents (Jarrett, J. Chromatogr., 1993, 618, 315-339). Chelating agents of the invention include but are not limited to disodium ethylenediaminetetraacetate (EDTA), citric acid, salicylates (e.g., sodium salicylate, 5-methoxysalicylate and homovanilate), N-acyl derivatives of collagen, laureth-9 and N-amino acyl derivatives of beta-diketones (enamines) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Buur et al., J. Control Rel., 1990, 14, 43-51).

[0140] Non-chelating non-surfactants: As used herein, non-chelating non-surfactant penetration enhancing compounds can be defined as compounds that demonstrate insignificant activity as chelating agents or as surfactants but that nonetheless enhance absorption of oligonucleotides through the alimentary mucosa (Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33). This class of penetration enhancers include, for example, unsaturated cyclic ureas, 1-alkyl- and 1-alkenylazacyclo-alkanone derivatives (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92); and non-steroidal anti-inflammatory agents such as diclofenac sodium, indomethacin and phenylbutazone (Yamashita et al., J. Pharm. Pharmacol., 1987, 39, 621-626).

[0141] Agents that enhance uptake of oligonucleotides at the cellular level may also be added to the pharmaceutical and other compositions of the present invention. For example, cationic lipids, such as lipofectin (Junichi et al, U.S. Pat. No. 5,705,188), cationic glycerol derivatives, and polycationic molecules, such as polylysine (Lollo et al., PCT Application WO 97/30731), are also known to enhance the cellular uptake of oligonucleotides.

[0142] Other agents may be utilized to enhance the penetration of the administered nucleic acids, including glycols such as ethylene glycol and propylene glycol, pyrrols such as 2-pyrrol, azones, and terpenes such as limonene and menthone.

[0143] Carriers

[0144] Certain compositions of the present invention also incorporate carrier compounds in the formulation. As used herein, “carrier compound” or “carrier” can refer to a nucleic acid, or analog thereof, which is inert (i.e., does not possess biological activity per se) but is recognized as a nucleic acid by in vivo processes that reduce the bioavailability of a nucleic acid having biological activity by, for example, degrading the biologically active nucleic acid or promoting its removal from circulation. The coadministration of a nucleic acid and a carrier compound, typically with an excess of the latter substance, can result in a substantial reduction of the amount of nucleic acid recovered in the liver, kidney or other extracirculatory reservoirs, presumably due to competition between the carrier compound and the nucleic acid for a common receptor. For example, the recovery of a partially phosphorothioate oligonucleotide in hepatic tissue can be reduced when it is coadministered with polyinosinic acid, dextran sulfate, polycytidic acid or 4-acetamido-4′isothiocyano-stilbene-2,2′-disulfonic acid (Miyao et al., Antisense Res. Dev., 1995, 5, 115-121; Takakura et al., Antisense & Nucl. Acid Drug Dev., 1996, 6, 177-183).

[0145] Excipients

[0146] In contrast to a carrier compound, a “pharmaceutical carrier” or “excipient” is a pharmaceutically acceptable solvent, suspending agent or any other pharmacologically inert vehicle for delivering one or more nucleic acids to an animal. The excipient may be liquid or solid and is selected, with the planned manner of administration in mind, so as to provide for the desired bulk, consistency, etc., when combined with a nucleic acid and the other components of a given pharmaceutical composition. Typical pharmaceutical carriers include, but are not limited to, binding agents (e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose, etc.); fillers (e.g., lactose and other sugars, microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethyl cellulose, polyacrylates or calcium hydrogen phosphate, etc.); lubricants (e.g., magnesium stearate, talc, silica, colloidal silicon dioxide, stearic acid, metallic stearates, hydrogenated vegetable oils, corn starch, polyethylene glycols, sodium benzoate, sodium acetate, etc.); disintegrants (e.g., starch, sodium starch glycolate, etc.); and wetting agents (e.g., sodium lauryl sulphate, etc.).

[0147] Pharmaceutically acceptable organic or inorganic excipient suitable for non-parenteral administration which do not deleteriously react with nucleic acids can also be used to formulate the compositions of the present invention. Suitable pharmaceutically acceptable carriers include, but are not limited to, water, salt solutions, alcohols, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

[0148] Formulations for topical administration of nucleic acids may include sterile and non-sterile aqueous solutions, non-aqueous solutions in common solvents such as alcohols, or solutions of the nucleic acids in liquid or solid oil bases. The solutions may also contain buffers, diluents and other suitable additives. Pharmaceutically acceptable organic or inorganic excipients suitable for non-parenteral administration which do not deleteriously react with nucleic acids can be used.

[0149] Suitable pharmaceutically acceptable excipients include, but are not limited to, water, salt solutions, alcohol, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

[0150] Other Components

[0151] The compositions of the present invention may additionally contain other adjunct components conventionally found in pharmaceutical compositions, at their art-established usage levels. Thus, for example, the compositions may contain additional, compatible, pharmaceutically-active materials such as, for example, antipruritics, astringents, local anesthetics or anti-inflammatory agents, or may contain additional materials useful in physically formulating various dosage forms of the compositions of the present invention, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers. However, such materials, when added, should not unduly interfere with the biological activities of the components of the compositions of the present invention. The formulations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the nucleic acid(s) of the formulation.

[0152] Aqueous suspensions may contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol and/or dextran. The suspension may also contain stabilizers.

[0153] Certain embodiments of the invention provide pharmaceutical compositions containing (a) one or more antisense compounds and (b) one or more other chemotherapeutic agents which function by a non-antisense mechanism. Examples of such chemotherapeutic agents include but are not limited to daunorubicin, daunomycin, dactinomycin, doxorubicin, epirubicin, idarubicin, esorubicin, bleomycin, mafosfamide, ifosfamide, cytosine arabinoside, bis-chloroethylnitrosurea, busulfan, mitomycin C, actinomycin D, mithramycin, prednisone, hydroxyprogesterone, testosterone, tamoxifen, dacarbazine, procarbazine, hexamethylmelamine, pentamethylmelamine, mitoxantrone, amsacrine, chlorambucil, methylcyclohexylnitrosurea, nitrogen mustards, melphalan, cyclophosphamide, 6-mercaptopurine, 6-thioguanine, cytarabine, 5-azacytidine, hydroxyurea, deoxycoformycin, 4-hydroxyperoxycyclophosphoramide, 5-fluorouracil (5-FU), 5-fluorodeoxyuridine (5-FUdR), methotrexate (MTX), colchicine, taxol, vincristine, vinblastine, etoposide (VP-16), trimetrexate, irinotecan, topotecan, gemcitabine, teniposide, cisplatin and diethylstilbestrol (DES). See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed. 1987, pp. 1206-1228, Berkow et al., eds., Rahway, N.J. When used with the compounds of the invention, such chemotherapeutic agents may be used individually (e.g., 5-FU and oligonucleotide), sequentially (e.g., 5-FU and oligonucleotide for a period of time followed by MTX and oligonucleotide), or in combination with one or more other such chemotherapeutic agents (e.g., 5-FU, MTX and oligonucleotide, or 5-FU, radiotherapy and oligonucleotide). Anti-inflammatory drugs, including but not limited to nonsteroidal anti-inflammatory drugs and corticosteroids, and antiviral drugs, including but not limited to ribivirin, vidarabine, acyclovir and ganciclovir, may also be combined in compositions of the invention. See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed., Berkow et al., eds., 1987, Rahway, N.J., pages 2499-2506 and 46-49, respectively). Other non-antisense chemotherapeutic agents are also within the scope of this invention. Two or more combined compounds may be used together or sequentially.

[0154] In another related embodiment, compositions of the invention may contain one or more antisense compounds, particularly oligonucleotides, targeted to a first nucleic acid and one or more additional antisense compounds targeted to a second nucleic acid target. Numerous examples of antisense compounds are known in the art. Two or more combined compounds may be used together or sequentially.

[0155] The formulation of therapeutic compositions and their subsequent administration is believed to be within the skill of those in the art. Dosing is dependent on severity and responsiveness of the disease state to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved. Optimal dosing schedules can be calculated-from measurements of drug accumulation in the body of the patient. Persons of ordinary skill can easily determine optimum dosages, dosing methodologies and repetition rates. Optimum dosages may vary depending on the relative potency of individual oligonucleotides, and can generally be estimated based on EC₅₀s found to be effective in in vitro and in vivo animal models. In general, dosage is from 0.01 ug to 100 g per kg of body weight, and may be given once or more daily, weekly, monthly or yearly, or even once every 2 to 20 years. Persons of ordinary skill in the art can easily estimate repetition rates for dosing based on measured residence times and concentrations of the drug in bodily fluids or tissues. Following successful treatment, it may be desirable to have the patient undergo maintenance therapy to prevent the recurrence of the disease state, wherein the oligonucleotide is administered in maintenance doses, ranging from 0.01 ug to 100 g per kg of body weight, once or more daily, to once every 20 years.

[0156] While the present invention has been described with specificity in accordance with certain of its preferred embodiments, the following examples serve only to illustrate the invention and are not intended to limit the same.

EXAMPLES Example 1

[0157] Nucleoside Phosphoramidites for Oligonucleotide Synthesis Deoxy and 2′-alkoxy amidites

[0158] 2′-Deoxy and 2′-methoxy beta-cyanoethyldiisopropyl phosphoramidites were purchased from commercial sources (e.g. Chemgenes, Needham Mass. or Glen Research, Inc. Sterling Va.). Other 2′-O-alkoxy substituted nucleoside amidites are prepared as described in U.S. Pat. No. 5,506,351, herein incorporated by reference. For oligonucleotides synthesized using 2′-alkoxy amidites, optimized synthesis cycles were developed that incorporate multiple steps coupling longer wait times relative to standard synthesis cycles.

[0159] The following abbreviations are used in the text: thin layer chromatography (TLC), melting point (MP), high pressure liquid chromatography (HPLC), Nuclear Magnetic Resonance (NMR), argon (Ar), methanol (MeOH), dichloromethane (CH₂Cl₂), triethylamine (TEA), dimethyl formamide (DMF), ethyl acetate (EtOAc), dimethyl sulfoxide (DMSO), tetrahydrofuran (THF).

[0160] Oligonucleotides containing 5-methyl-2′-deoxycytidine (5-Me-dC) nucleotides were synthesized according to published methods (Sanghvi, et. al., Nucleic Acids Research, 1993, 21, 3197-3203) using commercially available phosphoramidites (Glen Research, Sterling Va. or ChemGenes, Needham Mass.) or prepared as follows:

[0161] Preparation of 5′-O-Dimethoxytrityl-thymidine intermediate for 5-methyl dC amidite

[0162] To a 50 L glass reactor equipped with air stirrer and Ar gas line was added thymidine (1.00 kg, 4.13 mol) in anhydrous pyridine (6 L) at ambient temperature. Dimethoxytrityl (DMT) chloride (1.47 kg, 4.34 mol, 1.05 eq) was added as a solid in four portions over 1 h. After 30 min, TLC indicated approx. 95% product, 2% thymidine, 5% DMT reagent and by-products and 2 % 3′,5′-bis DMT product (R_(f) in EtOAc 0.45, 0.05, 0.98, 0.95 respectively). Saturated sodium bicarbonate (4 L) and CH₂Cl₂ were added with stirring (pH of the aqueous layer 7.5). An additional 18 L of water was added, the mixture was stirred, the phases were separated, and the organic layer was transferred to a second 50 L vessel. The aqueous layer was extracted with additional CH₂Cl₂ (2×2 L). The combined organic layer was washed with water (10 L) and then concentrated in a rotary evaporator to approx. 3.6 kg total weight. This was redissolved in CH₂Cl₂ (3.5 L), added to the reactor followed by water (6 L) and hexanes (13 L). The mixture was vigorously stirred and seeded to give a fine white suspended solid starting at the interface. After stirring for 1 h, the suspension was removed by suction through a ½″ diameter teflon tube into a 20 L suction flask, poured onto a 25 cm Coors Buchner funnel, washed with water (2×3 L) and a mixture of hexanes-CH₂Cl₂ (4:1, 2×3 L) and allowed to air dry overnight in pans (1″ deep). This was further dried in a vacuum oven (75° C., 0.1 mm Hg, 48 h) to a constant weight of 2072 g (93%) of a white solid, (mp 122-124° C). TLC indicated a trace contamination of the bis DMT product. NMR spectroscopy also indicated that 1-2 mole percent pyridine and about 5 mole percent of hexanes was still present.

[0163] Preparation of 5,-O-Dimethoxytrityl-2′-deoxy-5-methylcytidine intermediate for 5-methyl-dC amidite

[0164] To a 50 L Schott glass-lined steel reactor equipped with an electric stirrer, reagent addition pump (connected to an addition funnel), heating/cooling system, internal thermometer and an Ar gas line was added 5′-O-dimethoxytrityl-thymidine (3.00 kg, 5.51 mol), anhydrous acetonitrile (25 L) and TEA (12.3 L, 88.4 mol, 16 eq). The mixture was chilled with stirring to −10° C. internal temperature (external −20° C.). Trimethylsilylchloride (2.1 L, 16.5 mol, 3.0 eq) was added over 30 minutes while maintaining the internal temperature below −5° C., followed by a wash of anhydrous acetonitrile (1 L). Note: the reaction is mildly exothermic and copious hydrochloric acid fumes form over the course of the addition. The reaction was allowed to warm to 0° C. and the reaction progress was confirmed by TLC (EtOAc-hexanes 4:1; R_(f) 0.43 to 0.84 of starting material and silyl product, respectively). Upon completion, triazole (3.05 kg, 44 mol, 8.0 eq) was added the reaction was cooled to −20° C. internal temperature (external −30° C.). Phosphorous oxychloride (1035 mL, 11.1 mol, 2.01 eq) was added over 60 min so as to maintain the temperature between −20° C. and −10° C. during the strongly exothermic process, followed by a wash of anhydrous acetonitrile (1 L). The reaction was warmed to 0° C. and stirred for 1 h. TLC indicated a complete conversion to the triazole product (R_(f) 0.83 to 0.34 with the product spot glowing in long wavelength UV light). The reaction mixture was a peach-colored thick suspension, which turned darker red upon warming without apparent decomposition. The reaction was cooled to −15° C. internal temperature and water (5 L) was slowly added at a rate to maintain the temperature below +10° C. in order to quench the reaction and to form a homogenous solution. (Caution: this reaction is initially very strongly exothermic). Approximately one-half of the reaction volume (22 L) was transferred by air pump to another vessel, diluted with EtOAc (12 L) and extracted with water (2×8 L). The combined water layers were back-extracted with EtOAc (6 L). The water layer was discarded and the organic layers were concentrated in a 20 L rotary evaporator to an oily foam. The foam was coevaporated with anhydrous acetonitrile (4 L) to remove EtOAc. (note: dioxane may be used instead of anhydrous acetonitrile if dried to a hard foam). The second half of the reaction was treated in the same way. Each residue was dissolved in dioxane (3 L) and concentrated ammonium hydroxide (750 mL) was added. A homogenous solution formed in a few minutes and the reaction was allowed to stand overnight (although the reaction is complete within 1 h).

[0165] TLC indicated a complete reaction (product R_(f) 0.35 in EtOAc-MeOH 4:1). The reaction solution was concentrated on a rotary evaporator to a dense foam. Each foam was slowly redissolved in warm EtOAc (4 L; 50° C.), combined in a 50 L glass reactor vessel, and extracted with water (2×4L) to remove the triazole by-product. The water was back-extracted with EtOAc (2 L). The organic layers were combined and concentrated to about 8 kg total weight, cooled to 0° C. and seeded with crystalline product. After 24 hours, the first crop was collected on a 25 cm Coors Buchner funnel and washed repeatedly with EtOAc (3×3L) until a white powder was left and then washed with ethyl ether (2×3L). The solid was put in pans (1″ deep) and allowed to air dry overnight. The filtrate was concentrated to an oil, then redissolved in EtOAc (2 L), cooled and seeded as before. The second crop was collected and washed as before (with proportional solvents) and the filtrate was first extracted with water (2×1L) and then concentrated to an oil. The residue was dissolved in EtOAc (1 L) and yielded a third crop which was treated as above except that more washing was required to remove a yellow oily layer.

[0166] After air-drying, the three crops were dried in a vacuum oven (50° C., 0.1 mm Hg, 24 h) to a constant weight (1750, 600 and 200 g, respectively) and combined to afford 2550 g (85%) of a white crystalline product (MP 215-217° C.) when TLC and NMR spectroscopy indicated purity. The mother liquor still contained mostly product (as determined by TLC) and a small amount of triazole (as determined by NMR spectroscopy), bis DMT product and unidentified minor impurities. If desired, the mother liquor can be purified by silica gel chromatography using a gradient of MeOH (0-25%) in EtOAc to further increase the yield.

[0167] Preparation of 5′-O-Dimethoxytrityl-2′-deoxy-N4-benzoyl-5-methylcytidine penultimate intermediate for 5-methyl dC amidite

[0168] Crystalline 5′-O-dimethoxytrityl-5-methyl-2′-deoxycytidine (2000 g, 3.68 mol) was dissolved in anhydrous DMF (6.0 kg) at ambient temperature in a 50 L glass reactor vessel equipped with an air stirrer and argon line. Benzoic anhydride (Chem Impex not Aldrich, 874 g, 3.86 mol, 1.05 eq) was added and the reaction was stirred at ambient temperature for 8 h. TLC (CH₂Cl₂-EtOAc; CH₂Cl₂-EtOAc 4:1; R_(f) 0.25) indicated approx. 92% complete reaction. An additional amount of benzoic anhydride (44 g, 0.19 mol) was added. After a total of 18 h, TLC indicated approx. 96% reaction completion. The solution was diluted with EtOAc (20 L), TEA (1020 mL, 7.36 mol, ca 2.0 eq) was added with stirring, and the mixture was extracted with water (15 L, then 2×10 L). The aqueous layer was removed (no back-extraction was needed) and the organic layer was concentrated in 2×20 L rotary evaporator flasks until a foam began to form. The residues were coevaporated with acetonitrile (1.5 L each) and dried (0.1 mm Hg, 25° C., 24 h) to 2520 g of a dense foam. High pressure liquid chromatography (HPLC) revealed a contamination of 6.3% of N4, 3′-O-dibenzoyl product, but very little other impurities.

[0169] THe product was purified by Biotage column chromatography (5 kg Biotage) prepared with 65:35:1 hexanes-EtOAc-TEA (4L). The crude product (800 g), dissolved in CH₂Cl₂ (2 L), was applied to the column. The column was washed with the 65:35:1 solvent mixture (20 kg), then 20:80:1 solvent mixture (10 kg), then 99:1 EtOAc:TEA (17kg). The fractions containing the product were collected, and any fractions containing the product and impurities were retained to be resubjected to column chromatography. The column was re-equilibrated with the original 65:35:1 solvent mixture (17 kg). A second batch of crude product (840 g) was applied to the column as before. The column was washed with the following solvent gradients: 65:35:1 (9 kg), 55:45:1 (20 kg), 20:80:1 (10 kg), and 99:1 EtOAc:TEA(15 kg). The column was reequilibrated as above, and a third batch of the crude product (850 g) plus impure fractions recycled from the two previous columns (28 g) was purified following the procedure for the second batch. The fractions containing pure product combined and concentrated on a 20L rotary evaporator, co-evaporated with acetontirile (3 L) and dried (0.1 mm Hg, 48 h, 25° C.) to a constant weight of 2023 g (85%) of white foam and 20 g of slightly contaminated product from the third run. HPLC indicated a purity of 99.8% with the balance as the diBenzoyl product.

[0170] [5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-deoxy-N⁴-benzoyl-5-methylcytidin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite (5-methyl dC amidite)

[0171] 5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-deoxy-N⁴-benzoyl-5-methylcytidine (998 g, 1.5 mol) was dissolved in anhydrous DMF (2 L). The solution was co-evaporated with toluene (300 ml) at 50° C. under reduced pressure, then cooled to room temperature and 2-cyanoethyl tetraisopropylphosphorodiamidite (680 g, 2.26 mol) and tetrazole (52.5 g, 0.75 mol) were added. The mixture was shaken until all tetrazole was dissolved, N-methylimidazole (15 ml) was added and the mixture was left at room temperature for 5 hours. TEA (300 ml) was added, the mixture was diluted with DMF (2.5 L) and water (600 ml), and extracted with hexane (3×3 L). The mixture was diluted with water (1.2 L) and extracted with a mixture of toluene (7.5 L) and hexane (6 L). The two layers were separated, the upper layer was washed with DMF-water (7:3 v/v, 3×2 L) and water (3×2 L), and the phases were separated. The organic layer was dried (Na₂SO₄), filtered and rotary evaporated. The residue was co-evaporated with acetonitrile (2×2 L) under reduced pressure and dried to a constant weight (25° C., 0.1 mm Hg, 40 h) to afford 1250 g an off-white foam solid (96%).

[0172] 2′-Fluoro amidites

[0173] s2′-Fluorodeoxyadenosine amidites

[0174] 2′-fluoro oligonucleotides were synthesized as described previously [Kawasaki, et. al., J. Med. Chem., 1993, 36, 831-841] and U.S. Pat. No. 5,670,633, herein incorporated by reference. The preparation of 2′-fluoropyrimidines containing a 5-methyl substitution are described in U.S. Pat. No. 5,861,493. Briefly, the protected nucleoside N6-benzoyl-2′-deoxy-2′-fluoroadenosine was synthesized utilizing commercially available 9-beta-D-arabinofuranosyladenine as starting material and whereby the 2′-alpha-fluoro atom is introduced by a S_(N)2-displacement of a 2′-beta-triflate group. Thus N6-benzoyl-9-beta-D-arabinofuranosyladenine was selectively protected in moderate yield as the 3′,5′-ditetrahydropyranyl (THP) intermediate. Deprotection of the THP and N6-benzoyl groups was accomplished using standard methodologies to obtain the 5′-dimethoxytrityl-(DMT) and 5′-DMT-3′-phosphoramidite intermediates.

[0175] 2′-Fluorodeoxyguanosine

[0176] The synthesis of 2′-deoxy-2′-fluoroguanosine was accomplished using tetraisopropyldisiloxanyl (TPDS) protected 9-beta-D-arabinofuranosylguanine as starting material, and conversion to the intermediate isobutyryl-arabinofuranosylguanosine. Alternatively, isobutyryl-arabinofuranosylguanosine was prepared as described by Ross et al., (Nucleosides & Nucleosides, 16, 1645, 1997). Deprotection of the TPDS group was followed by protection of the hydroxyl group with THP to give isobutyryl di-THP protected arabinofuranosylguanine. Selective O -deacylation and triflation was followed by treatment of the crude product with fluoride, then deprotection of the THP groups. Standard methodologies were used to obtain the 5′-DMT- and 5′-DMT-3′-phosphoramidites.

[0177] 2′-Fluorouridine

[0178] Synthesis of 2′-deoxy-2′-fluorouridine was accomplished by the modification of a literature procedure in which 2,2′-anhydro-1-beta-D-arabinofuranosyluracil was treated with 70% hydrogen fluoride-pyridine. Standard procedures were used to obtain the 5′-DMT and 5′-DMT-3′phosphoramidites.

[0179] 2′-Fluorodeoxycytidine

[0180] 2′-deoxy-2′-fluorocytidine was synthesized via amination of 2′-deoxy-2′-fluorouridine, followed by selective protection to give N4-benzoyl-2′-deoxy-2′-fluorocytidine. Standard procedures were used to obtain the 5′-DMT and 5′-DMT-3′phosphoramidites.

[0181] 2′-0-(2-Methoxyethyl) Modified Amidites

[0182] 2′-O-Methoxyethyl-substituted nucleoside amidites (otherwise known as MOE amidites) are prepared as follows, or alternatively, as per the methods of Martin, P., (Helvetica Chimica Acta, 1995, 78, 486-504).

[0183] Preparation of 2′-0-(2-methoxyethyl)-5-methyluridine intermediate

[0184] 2,2′-Anhydro-5-methyl-uridine (2000 g, 8.32 mol), tris(2-methoxyethyl)borate (2504 g, 10.60 mol), sodium bicarbonate (60 g, 0.70 mol) and anhydrous 2-methoxyethanol (5 L) were combined in a 12 L three necked flask and heated to 130° C. (internal temp) at atmospheric pressure, under an argon atmosphere with stirring for 21 h. TLC indicated a complete reaction. The solvent was removed under reduced pressure until a sticky gum formed (50-85° C. bath temp and 100-11 mm Hg) and the residue was redissolved in water (3 L) and heated to boiling for 30 min in order the hydrolyze the borate esters. The water was removed under reduced pressure until a foam began to form and then the process was repeated. HPLC indicated about 77% product, 15% diner (5′ of product attached to 2′ of starting material) and unknown derivatives, and the balance was a single unresolved early eluting peak.

[0185] The gum was redissolved in brine (3 L), and the flask was rinsed with additional brine (3 L). The combined aqueous solutions were extracted with chloroform (20 L) in a heavier-than continuous extractor for 70 h. The chloroform layer was concentrated by rotary evaporation in a 20 L flask to a sticky foam (2400 g). This was coevaporated with MeOH (400 mL) and EtOAc (8 L) at 75° C. and 0.65 atm until the foam dissolved at which point the vacuum was lowered to about 0.5 atm. After 2.5 L of distillate was collected a precipitate began to form and the flask was removed from the rotary evaporator and stirred until the suspension reached ambient temperature. EtOAc (2 L) was added and the slurry was filtered on a 25 cm table top Buchner funnel and the product was washed with EtOAc (3×2 L). The bright white solid was air dried in pans for 24 h then further dried in a vacuum oven (50° C., 0.1 mm Hg, 24 h) to afford 1649 g of a white crystalline solid (mp 115.5-116.5° C.).

[0186] The brine layer in the 20 L continuous extractor was further extracted for 72 h with recycled chloroform. The chloroform was concentrated to 120 g of oil and this was combined with the mother liquor from the above filtration (225 g), dissolved in brine (250 mL) and extracted once with chloroform (250 mL). The brine solution was continuously extracted and the product was crystallized as described above to afford an additional 178 g of crystalline product containing about 2% of thymine. The combined yield was 1827 g (69.4%). HPLC indicated about 99.5% purity with the balance being the diner.

[0187] Preparation of 5′-O-DMT-2′-O-(2-methoxyethyl)-5-methyluridine penultimate intermediate

[0188] In a 50 L glass-lined steel reactor, 2′-O-(2-methoxyethyl)-5-methyl-uridine (MOE-T, 1500 g, 4.738 mol), lutidine (1015 g, 9.476 mol) were dissolved in anhydrous acetonitrile (15 L). The solution was stirred rapidly and chilled to −10° C. (internal temperature). Dimethoxytriphenylmethyl chloride (1765.7 g, 5.21 mol) was added as a solid in one portion. The reaction was allowed to warm to −2° C. over 1 h. (Note: The reaction was monitored closely by TLC (EtOAc) to determine when to stop the reaction so as to not generate the undesired bis-DMT substituted side product). The reaction was allowed to warm from −2 to 3° C. over 25 min. then quenched by adding MeOH (300 mL) followed after 10 min by toluene (16 L) and water (16 L). The solution was transferred to a clear 50 L vessel with a bottom outlet, vigorously stirred for 1 minute, and the layers separated. The aqueous layer was removed and the organic layer was washed successively with 10% aqueous citric acid (8 L) and water (12 L). The product was then extracted into the aqueous phase by washing the toluene solution with aqueous sodium hydroxide (0.5N, 16 L and 8 L). The combined aqueous layer was overlayed with toluene (12 L) and solid citric acid (8 moles, 1270 g) was added with vigorous stirring to lower the pH of the aqueous layer to 5.5 and extract the product into the toluene. The organic layer was washed with water (10 L) and TLC of the organic layer indicated a trace of DMT-O-Me, bis DMT and dimer DMT.

[0189] The toluene solution was applied to a silica gel column (6 L sintered glass funnel containing approx. 2 kg of silica gel slurried with toluene (2 L) and TEA(25 mL)) and the fractions were eluted with toluene (12 L) and EtOAc (3×4 L) using vacuum applied to a filter flask placed below the column. The first EtOAc fraction containing both the desired product and impurities were resubjected to column chromatography as above. The clean fractions were combined, rotary evaporated to a foam, coevaporated with acetonitrile (6 L) and dried in a vacuum oven (0.1 mm Hg, 40 h, 40° C.) to afford 2850 g of a white crisp foam. NMR spectroscopy indicated a 0.25 mole % remainder of acetonitrile (calculates to be approx. 47 g) to give a true dry weight of 2803 g (96%). HPLC indicated that the product was 99.41% pure, with the remainder being 0.06 DMT-O-Me, 0.10 unknown, 0.44 bis DMT, and no detectable dimer DMT or 3′-O-DMT.

[0190] Preparation of [5′-0-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-5-methyluridin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite (MOE T amidite)

[0191] 5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-5-methyluridine (1237 g, 2.0 mol) was dissolved in anhydrous DMF (2.5 L). The solution was co-evaporated with toluene (200 ml) at 50° C. under reduced pressure, then cooled to room temperature and 2-cyanoethyl tetraisopropylphosphorodiamidite (900 g, 3.0 mol) and tetrazole (70 g, 1.0 mol) were added. The mixture was shaken until all tetrazole was dissolved, N-methylimidazole (20 ml) was added and the solution was left at room temperature for 5 hours. TEA (300 ml) was added, the mixture was diluted with DMF (3.5 L) and water (600 ml) and extracted with hexane (3×3L). The mixture was diluted with water (1.6 L) and extracted with the mixture of toluene (12 L) and hexanes (9 L). The upper layer was washed with DMF-water (7:3 v/v, 3×3 L) and water (3×3 L). The organic layer was dried (Na₂SO₄), filtered and evaporated. The residue was co-evaporated with acetonitrile (2×2 L) under reduced pressure and dried in a vacuum oven (25° C., 0.1 mm Hg, 40 h) to afford 1526 g of an off-white foamy solid (95%).

[0192] Preparation of 5′-O-Dimethoxytrityl-2′-O-(2-methoxyethyl)-5-methylcytidine intermediate

[0193] To a 50 L Schott glass-lined steel reactor equipped with an electric stirrer, reagent addition pump (connected to an addition funnel), heating/cooling system, internal thermometer and argon gas line was added 5′-O-dimethoxytrityl-2′-O-(2-methoxyethyl)-5-methyl-uridine (2.616 kg, 4.23 mol, purified by base extraction only and no scrub column), anhydrous acetonitrile (20 L), and TEA (9.5 L, 67.7 mol, 16 eq). The mixture was chilled with stirring to −10° C. internal temperature (external −20° C.). Trimethylsilylchloride (1.60 L, 12.7 mol, 3.0 eq) was added over 30 min. while maintaining the internal temperature below −5° C., followed by a wash of anhydrous acetonitrile (1 L). (Note: the reaction is mildly exothermic and copious hydrochloric acid fumes form over the course of the addition). The reaction was allowed to warm to 0° C. and the reaction progress was confirmed by TLC (EtOAc, R_(f) 0.68 and 0.87 for starting material and silyl product, respectively). Upon completion, triazole (2.34 kg, 33.8 mol, 8.0 eq) was added the reaction was cooled to −20° C. internal temperature (external −30° C.). Phosphorous oxychloride (793 mL, 8.51 mol, 2.01 eq) was added slowly over 60 min so as to maintain the temperature between −20° C. and −10° C. (note: strongly exothermic), followed by a wash of anhydrous acetonitrile (1 L). The reaction was warmed to 0° C. and stirred for 1 h, at which point it was an off-white thick suspension. TLC indicated a complete conversion to the triazole product (EtOAc, R_(f) 0.87 to 0.75 with the product spot glowing in long wavelength UV light). The reaction was cooled to −15° C. and water (5 L) was slowly added at a rate to maintain the temperature below +10° C. in order to quench the reaction and to form a homogenous solution. (Caution: this reaction is initially very strongly exothermic). Approximately one-half of the reaction volume (22 L) was transferred by air pump to another vessel, diluted with EtOAc (12 L) and extracted with water (2×8 L). The second half of the reaction was treated in the same way. The combined aqueous layers were back-extracted with EtOAc (8 L) The organic layers were combined and concentrated in a 20 L rotary evaporator to an oily foam. The foam was coevaporated with anhydrous acetonitrile (4 L) to remove EtOAc. (note: dioxane may be used instead of anhydrous acetonitrile if dried to a hard foam). The residue was dissolved in dioxane (2 L) and concentrated ammonium hydroxide (750 mL) was added. A homogenous solution formed in a few minutes and the reaction was allowed to stand overnight.

[0194] TLC indicated a complete reaction (CH₂Cl₂-acetone-MeOH, 20:5:3, R_(f) 0.51). The reaction solution was concentrated on a rotary evaporator to a dense foam and slowly redissolved in warm CH₂Cl₂ (4 L, 40° C.) and transferred to a 20 L glass extraction vessel equipped with a air-powered stirrer. The organic layer was extracted with water (2×6 L) to remove the triazole by-product. (Note: In the first extraction an emulsion formed which took about 2 h to resolve). The water layer was back-extracted with CH₂Cl₂ (2×2 L), which in turn was washed with water (3 L). The combined organic layer was concentrated in 2×20 L flasks to a gum and then recrystallized from EtOAc seeded with crystalline product. After sitting overnight, the first crop was collected on a 25 cm Coors Buchner funnel and washed repeatedly with EtOAc until a white free-flowing powder was left (about 3×3 L). The filtrate was concentrated to an oil recrystallized from EtOAc, and collected as above. The solid was air-dried in pans for 48 h, then further dried in a vacuum oven (50° C., 0.1 mm Hg, 17 h) to afford 2248 g of a bright white, dense solid (86%). An HPLC analysis indicated both crops to be 99.4% pure and NMR spectroscopy indicated only a faint trace of EtOAc remained.

[0195] Preparation of 5′-O-dimethoxytrityl-2′-O-(2-methoxyethyl)-N4-benzoyl-5-methyl-cytidine penultimate intermediate:

[0196] Crystalline 5′-O-dimethoxytrityl-2′-O-(2-methoxyethyl)-5-methyl-cytidine (1000 g, 1.62 mol) was suspended in anhydrous DMF (3 kg) at ambient temperature and stirred under an Ar atmosphere. Benzoic anhydride (439.3 g, 1.94 mol) was added in one portion. The solution clarified after 5 hours and was stirred for 16 h. HPLC indicated 0.45% starting material remained (as well as 0.32% N4, 3′-O-bis Benzoyl). An additional amount of benzoic anhydride (6.0 g, 0.0265 mol) was added and after 17 h, HPLC indicated no starting material was present. TEA (450 mL, 3.24 mol) and toluene (6 L) were added with stirring for 1 minute. The solution was washed with water (4×4 L), and brine (2×4 L). The organic layer was partially evaporated on a 20 L rotary evaporator to remove 4 L of toluene and traces of water. HPLC indicated that the bis benzoyl side product was present as a 6% impurity. The residue was diluted with toluene (7 L) and anhydrous DMSO (200 mL, 2.82 mol) and sodium hydride (60% in oil, 70 g, 1.75 mol) was added in one portion with stirring at ambient temperature over 1 h. The reaction was quenched by slowly adding then washing with aqueous citric acid (10%, 100 mL over 10 min, then 2×4 L), followed by aqueous sodium bicarbonate (2%, 2 L), water (2×4 L) and brine (4 L). The organic layer was concentrated on a 20 L rotary evaporator to about 2 L total volume. The residue was purified by silica gel column chromatography (6 L Buchner funnel containing 1.5 kg of silica gel wetted with a solution of EtOAc-hexanes-TEA(70:29:1)). The product was eluted with the same solvent (30 L) followed by straight EtOAc (6 L). The fractions containing the product were combined, concentrated on a rotary evaporator to a foam and then dried in a vacuum oven (50° C., 0.2 mm Hg, 8 h) to afford 1155 g of a crisp, white foam (98%). HPLC indicated a purity of >99.7%.

[0197] Preparation of [5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl) -N⁴-benzoyl-5-methylcytidin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite (MOE 5-Me-C amidite)

[0198] 5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-N⁴-benzoyl-5-methylcytidine (1082 g, 1.5 mol) was dissolved in anhydrous DMF (2 L) and co-evaporated with toluene (300 ml) at 50° C. under reduced pressure. The mixture was cooled to room temperature and 2-cyanoethyl tetraisopropylphosphorodiamidite (680 g, 2.26 mol) and tetrazole (52.5 g, 0.75 mol) were added. The mixture was shaken until all tetrazole was dissolved, N-methylimidazole (30 ml) was added, and the mixture was left at room temperature for 5 hours. TEA (300 ml) was added, the mixture was diluted with DMF (1 L) and water (400 ml) and extracted with hexane (3×3 L). The mixture was diluted with water (1.2 L) and extracted with a mixture of toluene (9 L) and hexanes (6 L). The two layers were separated and the upper layer was washed with DMF-water (60:40 v/v, 3×3 L) and water (3×2 L). The organic layer was dried (Na₂SO₄), filtered and evaporated. The residue was co-evaporated with acetonitrile (2×2 L) under reduced pressure and dried in a vacuum oven (25° C., 0.1 mm Hg, 40 h) to afford 1336 g of an off-white foam (97%).

[0199] Preparation of [5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl) -N⁶-benzoyladenosin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite (MOE A amdite)

[0200] 5′-O-(4,4′-Dimethoxytriphenylmethyl) -2′-O-(2-methoxyethyl)-N⁶-benzoyladenosine (purchased from Reliable Biopharmaceutical, St. Lois, Mo.), 1098 g, 1.5 mol) was dissolved in anhydrous DMF (3 L) and co-evaporated with toluene (300 ml) at 50 ° C. The mixture was cooled to room temperature and 2-cyanoethyl tetraisopropylphosphorodiamidite (680 g, 2.26 mol) and tetrazole (78.8 g, 1.24 mol) were added. The mixture was shaken until all tetrazole was dissolved, N-methylimidazole (30 ml) was added, and mixture was left at room temperature for 5 hours. TEA (300 ml) was added, the mixture was diluted with DMF (1 L) and water (400 ml) and extracted with hexanes (3×3 L). The mixture was diluted with water (1.4 L) and extracted with the mixture of toluene (9 L) and hexanes (6 L) . The two layers were separated and the upper layer was washed with DMF-water (60:40, v/v, 3×3 L) and water (3×2 L). The organic layer was dried (Na₂SO₄), filtered and evaporated to a sticky foam. The residue was co-evaporated with acetonitrile (2.5 L) under reduced pressure and dried in a vacuum oven (25° C., 0.1 mm Hg, 40 h) to afford 1350 g of an off-white foam solid (96%).

[0201] Prepartion of [5′-O-(4,41-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl) -N⁴-isobutyrylguanosin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite (MOE G amidite)

[0202] 5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-N⁴-isobutyrlguanosine (purchased from Reliable Biopharmaceutical, St. Louis, Mo., 1426 g, 2.0 mol) was dissolved in anhydrous DMF (2 L). The solution was co-evaporated with toluene (200 ml) at 50 ° C., cooled to room temperature and 2-cyanoethyl tetraisopropylphosphorodiamidite (900 g, 3.0 mol) and tetrazole (68 g, 0.97 mol) were added. The mixture was shaken until all tetrazole was dissolved, N-methylimidazole (30 ml) was added, and the mixture was left at room temperature for 5 hours. TEA (300 ml) was added, the mixture was diluted with DMF (2 L) and water (600 ml) and extracted with hexanes (3×3 L). The mixture was diluted with water (2 L) and extracted with a mixture of toluene (10 L) and hexanes (5 L) . The two layers were separated and the upper layer was washed with DMF-water (60:40, v/v, 3×3 L). EtOAc (4 L) was added and the solution was washed with water (3×4 L). The organic layer was dried (Na₂SO₄), filtered and evaporated to approx. 4 kg. Hexane (4 L) was added, the mixture was shaken for 10 min, and the supernatant liquid was decanted. The residue was co-evaporated with acetonitrile (2×2 L) under reduced pressure and dried in a vacuum oven (25° C., 0.1 mm Hg, 40 h) to afford 1660 g of an off-white foamy solid (91%).

[0203] 2′-O-(Aminooxyethyl) nucleoside amidites and 2′-O-(dimethylaminooxyethyl) nucleoside amidites

[0204] 2′-(Dimethylaminooxyethoxy) nucleoside amidites

[0205] 2′-(Dimethylaminooxyethoxy) nucleoside amidites (also known in the art as 2′-O-(dimethylaminooxyethyl) nucleoside amidites) are prepared as described in the following paragraphs. Adenosine, cytidine and guanosine nucleoside amidites are prepared similarly to the thymidine (5-methyluridine) except the exocyclic amines are protected with a benzoyl moiety in the case of adenosine and cytidine and with isobutyryl in the case of guanosine.

[0206] 5′-O-tert-Butyldiphenylsilyl-O²-2′-anhydro-5-methyluridine

[0207] O²-2′-anhydro-5-methyluridine (Pro. Bio. Sint., Varese, Italy, 100.0 g, 0.416 mmol), dimethylaminopyridine (0.66 g, 0.013 eq, 0.0054 mmol) were dissolved in dry pyridine (500 ml) at ambient temperature under an argon atmosphere and with mechanical stirring. tert-Butyldiphenylchlorosilane (125.8 g, 119.0 mL, 1.1 eq, 0.458 mmol) was added in one portion. The reaction was stirred for 16 h at ambient temperature. TLC (R_(f) 0.22, EtOAc) indicated a complete reaction. The solution was concentrated under reduced pressure to a thick oil. This was partitioned between CH₂Cl₂ (1 L) and saturated sodium bicarbonate (2×1 L) and brine (1 L). The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure to a thick oil. The oil was dissolved in a 1:1 mixture of EtOAc and ethyl ether (600 mL) and cooling the solution to −10° C. afforded a white crystalline solid which was collected by filtration, washed with ethyl ether (3×2 00 mL) and dried (40° C., 1 mm Hg, 24 h) to afford 149 g of white solid (74.8%). TLC and NMR spectroscopy were consistent with pure product.

[0208] 5′-O-tert-Butyldiphenylsilyl-2′-O-(2-hydroxyethyl)-5-methyluridine

[0209] In the fume hood, ethylene glycol (350 mL, excess) was added cautiously with manual stirring to a 2 L stainless steel pressure reactor containing borane in tetrahydrofuran (1.0 M, 2.0 eq, 622 mL). (Caution : evolves hydrogen gas). 5′-O-tert-Butyldiphenylsilyl-O²-2′-anhydro-5-methyluridine (149 g, 0.311 mol) and sodium bicarbonate (0.074 g, 0.003 eq) were added with manual stirring. The reactor was sealed and heated in an oil bath until an internal temperature of 160 ° C. was reached and then maintained for 16 h (pressure <100 psig). The reaction vessel was cooled to ambient temperature and opened. TLC (EtOAc, R_(f) 0.67 for desired product and R_(f) 0.82 for ara-T side product) indicated about 70% conversion to the product. The solution was concentrated under reduced pressure (10 to 1 mm Hg) in a warm water bath (40-100° C.) with the more extreme conditions used to remove the ethylene glycol. (Alternatively, once the THF has evaporated the solution can be diluted with water and the product extracted into EtOAc). The residue was purified by column chromatography (2 kg silica gel, EtOAc-hexanes gradient 1:1 to 4:1). The appropriate fractions were combined, evaporated and-dried to afford 84 g of a white crisp foam (50%), contaminated starting material (17.4 g, 12% recovery) and pure reusable starting material (20 g, 13% recovery). TLC and NMR spectroscopy were consistent with 99% pure product.

[0210] 2′-O-([2-phthalimidoxy)ethyl]-5′-t-butyldiphenylsilyl-5-methyluridine

[0211] 5′-O-tert-Butyldiphenylsilyl-2′-O-(2-hydroxyethyl)-5-methyluridine (20 g, 36.98 mmol) was mixed with triphenylphosphine (11.63 g, 44.36 mmol) and N-hydroxyphthalimide (7.24 g, 44.36 mmol) and dried over P₂O₅ under high vacuum for two days at 40° C. The reaction mixture was flushed with argon and dissolved in dry THF (369.8 mL, Aldrich, sure seal bottle). Diethyl-azodicarboxylate (6.98 mL, 44.36 mmol) was added dropwise to the reaction mixture with the rate of addition maintained such that the resulting deep red coloration is just discharged before adding the next drop. The reaction mixture was stirred for 4 hrs., after which time TLC (EtOAc:hexane, 60:40) indicated that the reaction was complete. The solvent was evaporated in vacuuo and the residue purified by flash column chromatography (eluted with 60:40 EtOAc:hexane), to yield 2′-O-([2-phthalimidoxy)ethyl]-5′-t-butyldiphenylsilyl-5-methyluridine as white foam (21.819 g, 86%) upon rotary evaporation.

[0212] 5′-O-tert-butyldiphenylsilyl-2′-O-[(2-formadoximinooxy)ethyl]-5-methyluridine

[0213] 2′-O-([2-phthalimidoxy)ethyl]-5′-t-butyldiphenylsilyl-5-methyluridine (3.1 g, 4.5 mmol) was dissolved in dry CH₂Cl₂ (4.5 mL) and methylhydrazine (300 mL, 4.64 mmol) was added dropwise at −10° C. to 0° C. After 1 h the mixture was filtered, the filtrate washed with ice cold CH₂Cl₂, and the combined organic phase was washed with water and brine and dried (anhydrous Na₂SO₄). The solution was filtered and evaporated to afford 2′-O-(aminooxyethyl) thymidine, which was then dissolved in MeOH (67.5 mL). Formaldehyde (20% aqueous solution, w/w, 1.1 eq.) was added and the resulting mixture was stirred for 1 h. The solvent was removed under vacuum and the residue was purified by column chromatography to yield 5′-O-tert-butyldiphenylsilyl-2′-O-[(2-formadoximinooxy) ethyl]-5-methyluridine as white foam (1.95 g, 78%) upon rotary evaporation.

[0214] 5′-O-tert-Butyldiphenylsilyl-2′-O-[N,N dimethylaminooxyethyl]-5-methyluridine

[0215] 5′-O-tert-butyldiphenylsilyl-2′-O-[(2-formadoximinooxy)ethyl]-5-methyluridine (1.77 g, 3.12 mmol) was dissolved in a solution of 1M pyridinium p-toluenesulfonate (PPTS) in dry MeOH (30.6 mL) and cooled to 10° C. under inert atmosphere. Sodium cyanoborohydride (0.39 g, 6.13 mmol) was added and the reaction mixture was stirred. After 10 minutes the reaction was warmed to room temperature and stirred for 2 h. while the progress of the reaction was monitored by TLC (5% MeOH in CH₂Cl₂). Aqueous NaHCO₃ solution (5%, 10 mL) was added and the product was extracted with EtOAc (2×20 mL). The organic phase was dried over anhydrous Na₂SO₄, filtered, and evaporated to dryness. This entire procedure was repeated with the resulting residue, with the exception that formaldehyde (20% w/w, 30 mL, 3.37 mol) was added upon dissolution of the residue in the PPTS/MeOH solution. After the extraction and evaporation, the residue was purified by flash column chromatography and (eluted with 5% MeOH in CH₂Cl₂) to afford 5′-O-tert-butyldiphenylsilyl-2′-O-[N,N-dimethylaminooxyethyl]-5-methyluridine as a white foam (14.6 g, 80%) upon rotary evaporation.

[0216] 2′-O-(dimethylaminooxyethyl)-5-methyluridine

[0217] Triethylamine trihydrofluoride (3.91 mL, 24.0 mmol) was dissolved in dry THF and TEA (1.67 mL, 12 mmol, dry, stored over KOH) and added to 5′-O-tert-butyldiphenylsilyl-2′-O-[N,N-dimethylaminooxyethyl]-5-methyluridine (1.40 g, 2.4 mmol). The reaction was stirred at room temperature for 24 hrs and monitored by TLC (5% MeOH in CH₂Cl₂). The solvent was removed under vacuum and the residue purified by flash column chromatography (eluted with 10% MeOH in CH₂Cl₂) to afford 2′-O-(dimethylaminooxyethyl)-5-methyluridine (766 mg, 92.5%) upon rotary evaporation of the solvent.

[0218] 5′-O-DMT-2′-O-(dimethylaminooxyethyl)-5-methyluridine

[0219] 2′-0-(dimethylaminooxyethyl)-5-methyluridine (750 mg, 2.17 mmol) was dried over P₂O₅ under high vacuum overnight at 40° C., co-evaporated with anhydrous pyridine (20 mL), and dissolved in pyridine (11 mL) under argon atmosphere. 4-dimethylaminopyridine (26.5 mg, 2.60 mmol) and 4,4′-dimethoxytrityl chloride (880 mg, 2.60 mmol) were added to the pyridine solution and the reaction mixture was stirred at room temperature until all of the starting material had reacted. Pyridine was removed under vacuum and the residue was purified by column chromatography (eluted with 10% MeOH in CH₂Cl₂ containing a few drops of pyridine) to yield 5′-O-DMT-2′-O-(dimethylamino-oxyethyl)-5-methyluridine (1.13 g, 80%) upon rotary evaporation.

[0220] 5′-O-DmT-2′-O-(2-N,N-dimethylaminooxyethyl)-5-methyluridine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite]

[0221] 5′-O-DMT-2′-O-(dimethylaminooxyethyl)-5-methyluridine (1.08 g, 1.67 mmol) was co-evaporated with toluene (20 mL), N,N-diisopropylamine tetrazonide (0.29 g, 1.67 mmol) was added and the mixture was dried over P₂O₅ under high vacuum overnight at 40° C. This was dissolved in anhydrous acetonitrile (8.4 mL) and 2-cyanoethyl-N,N,N¹,N¹-tetraisopropylphosphoramidite (2.12 mL, 6.08 mmol) was added. The reaction mixture was stirred at ambient temperature for 4 h under inert atmosphere. The progress of the reaction was monitored by TLC (hexane:EtOAc 1:1). The solvent was evaporated, then the residue was dissolved in EtOAc (70 mL) and washed with 5% aqueous NaHCO₃ (40 mL). The EtOAc layer was dried over anhydrous Na₂SO₄, filtered, and concentrated. The residue obtained was purified by column chromatography (EtOAc as eluent) to afford 5′-O-DMT-2′-O-(2-N,N-dimethylaminooxyethyl)-5-methyluridine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite] as a foam (1.04 g, 74.9%) upon rotary evaporation.

[0222] 2′-(Aminooxyethoxy) nucleoside amidites

[0223] 2′-(Aminooxyethoxy) nucleoside amidites (also known in the art as 2′-O-(aminooxyethyl) nucleoside amidites) are prepared as described in the following paragraphs. Adenosine, cytidine and thymidine nucleoside amidites are prepared similarly.

[0224] N2-isobutyryl-6-O-diphenylcarbamoyl-2′-O-(2-ethylacetyl)-5′-O-(4,4′-dimethoxytrityl)guanosine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite]

[0225] The 2′-O-aminooxyethyl guanosine analog may be obtained by selective 2′-O-alkylation of diaminopurine riboside. Multigram quantities of diaminopurine riboside may be purchased from Schering AG (Berlin) to provide 2′-O-(2-ethylacetyl) diaminopurine riboside along with a minor amount of the 3′-O-isomer. 2′-O-(2-ethylacetyl) diaminopurine riboside may be resolved and converted to 2′-O-(2-ethylacetyl)guanosine by treatment with adenosine deaminase. (McGee, D. P. C., Cook, P. D., Guinosso, C. J., WO 94/02501 A1 940203.) Standard protection procedures should afford 2′-O-(2-ethylacetyl)-5′-O-(4,4′-dimethoxytrityl)guanosine and 2-N-isobutyryl-6-O-diphenylcarbamoyl-2′-O-(2-ethylacetyl)-5′-O-(4,4′-dimethoxytrityl)guanosine which may be reduced to provide 2-N-isobutyryl-6-O-diphenylcarbamoyl-2′-O-(2-hydroxyethyl)-5′-O-(4,4′-dimethoxytrityl)guanosine. As before the hydroxyl group may be displaced by N-hydroxyphthalimide via a Mitsunobu reaction, and the protected nucleoside may be phosphitylated as usual to yield 2-N-isobutyryl-6-O-diphenylcarbamoyl-2′-O-([2-phthalmidoxy]ethyl)-5′-O-(4,4′-dimethoxytrityl)guanosine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite].

[0226] 2′-dimethylaminoethoxyethoxy (2′-DMAEOE) nucleoside amidites

[0227] 2′-dimethylaminoethoxyethoxy nucleoside amidites (also known in the art as 2′-O-dimethylaminoethoxyethyl, i.e., 2′-O—CH₂—O—CH₂—N(CH₂)₂, or 2′-DMAEOE nucleoside amidites) are prepared as follows. Other nucleoside amidites are prepared similarly.

[0228] 2′-O-[2(2-N,N-dimethylaminoethoxy)ethyl]-5-methyl uridine

[0229] 2[2-(Dimethylamino)ethoxy]ethanol (Aldrich, 6.66 g, 50 mmol) was slowly added to a solution of borane in tetra-hydrofuran (1 M, 10 mL, 10 mmol) with stirring in a 100 mL bomb. (Caution: Hydrogen gas evolves as the solid dissolves). O²-,2′-anhydro-5-methyluridine (1.2 g, 5 mmol), and sodium bicarbonate (2.5 mg) were added and the bomb was sealed, placed in an oil bath and heated to 155° C. for 26 h. then cooled to room temperature. The crude solution was concentrated, the residue was diluted with water (200 mL) and extracted with hexanes (200 mL). The product was extracted from the aqueous layer with EtOAc (3×200 mL) and the combined organic layers were washed once with water, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (eluted with 5:100:2 MeOH/CH₂Cl₂/TEA) as the eluent. The appropriate fractions were combined and evaporated to afford the product as a white solid.

[0230] 5 5′-O-dimethoxytrityl-2′-O-[2(2-N,N-dimethylaminoethoxy) ethyl)]-5-methyl uridine

[0231] To 0.5 g (1.3 mmol) of 2′-O-[2(2-N,N-dimethylamino-ethoxy)ethyl)]-5-methyl uridine in anhydrous pyridine (8 mL), was added TEA (0.36 mL) and dimethoxytrityl chloride (DMT-Cl, 0.87 g, 2 eq.) and the reaction was stirred for 1 h. The reaction mixture was poured into water (200 mL) and extracted with CH₂Cl₂ (2×200 mL). The combined CH₂Cl₂ layers were washed with saturated NaHCO₃ solution, followed by saturated NaCl solution, dried over anhydrous sodium sulfate, filtered and evaporated. The residue was purified by silica gel column chromatography (eluted with 5:100:1 MeOH/CH₂Cl₂/TEA) to afford the product.

[0232] 5′-O-Dimethoxytrityl-2′-O-[2(2-N,N-dimethylaminoethoxy)-ethyl)]-5-methyl uridine-3 ′-O-(cyanoethyl-N,N-diisopropyl)phosphoramidite

[0233] Diisopropylaminotetrazolide (0.6 g) and 2-cyanoethoxy-N,N-diisopropyl phosphoramidite (1.1 mL, 2 eq.) were added to a solution of 5′-O-dimethoxytrityl-2′-O-[2(2-N,N-dimethylaminoethoxy)ethyl)]-5-methyluridine (2.17 g, 3 mmol) dissolved in CH₂Cl₂ (20 mL) under an atmosphere of argon. The reaction mixture was stirred overnight and the solvent evaporated. The resulting residue was purified by silica gel column chromatography with EtOAc as the eluent to afford the title compound.

Example 2

[0234] Oligonucleotide Synthesis

[0235] Unsubstituted and substituted phosphodiester (P═O) oligonucleotides are synthesized on an automated DNA synthesizer (Applied Biosystems model 394) using standard phosphoramidite chemistry with oxidation by iodine.

[0236] Phosphorothioates (P═S) are synthesized similar to phosphodiester oligonucleotides with the following exceptions: thiation was effected by utilizing a 10% w/v solution of 3H-1,2-benzodithiole-3-one 1,1-dioxide in acetonitrile for the oxidation of the phosphite linkages. The thiation reaction step time was increased to 180 sec and preceded by the normal capping step. After cleavage from the CPG column and deblocking in concentrated ammonium hydroxide at 55° C. (12-16 hr), the oligonucleotides were recovered by precipitating with >3 volumes of ethanol from a 1 M NH₄oAc solution. Phosphinate oligonucleotides are prepared as described in U.S. Pat. No. 5,508,270, herein incorporated by reference.

[0237] Alkyl phosphonate oligonucleotides are prepared as described in U.S. Pat. No. 4,469,863, herein incorporated by reference.

[0238] 3′-Deoxy-3′-methylene phosphonate oligonucleotides are prepared as described in U.S. Pat. Nos. 5,610,289 or 5,625,050, herein incorporated by reference.

[0239] Phosphoramidite oligonucleotides are prepared as described in U.S. Pat. No. 5,256,775 or U.S. Pat. No. 5,366,878, herein incorporated by reference.

[0240] Alkylphosphonothioate oligonucleotides are prepared as described in published PCT applications PCT/US94/00902 and PCT/US93/06976 (published as WO 94/17093 and WO 94/02499, respectively), herein incorporated by reference.

[0241] 3′-Deoxy-3′-amino phosphoramidate oligonucleotides are prepared as described in U.S. Pat. No. 5,476,925, herein incorporated by reference.

[0242] Phosphotriester oligonucleotides are prepared as described in U.S. Pat. No. 5,023,243, herein incorporated by reference.

[0243] Borano phosphate oligonucleotides are prepared as described in U.S. Pat. Nos. 5,130,302 and 5,177,198, both herein incorporated by reference.

Example 3

[0244] Oligonucleoside Synthesis

[0245] Methylenemethylimino linked oligonucleosides, also identified as MMI linked oligonucleosides, methylenedimethyl-hydrazo linked oligonucleosides, also identified as MDH linked oligonucleosides, and methylenecarbonylamino linked oligonucleosides, also identified as amide-3 linked oligonucleosides, and methyleneaminocarbonyl linked oligo-nucleosides, also identified as amide-4 linked oligonucleo-sides, as well as mixed backbone compounds having, for instance, alternating MMI and P═O or P═S linkages are prepared as described in U.S. Pat. Nos. 5,378,825, 5,386,023, 5,489,677, 5,602,240 and 5,610,289, all of which are herein incorporated by reference.

[0246] Formacetal and thioformacetal linked oligonucleosides are prepared as described in U.S. Pat. Nos. 5,264,562 and 5,264,564, herein incorporated by reference.

[0247] Ethylene oxide linked oligonucleosides are prepared as described in U.S. Pat. No. 5,223,618, herein incorporated by reference.

Example 4

[0248] PNA Synthesis

[0249] Peptide nucleic acids (PNAs) are prepared in accordance with any of the various procedures referred to in Peptide Nucleic Acids (PNA): Synthesis, Properties and Potential Applications, Bioorganic & Medicinal Chemistry, 1996, 4, 5-23. They may also be prepared in accordance with U.S. Pat. Nos. 5,539,082, 5,700,922, and 5,719,262, herein incorporated by reference.

Example 5

[0250] Synthesis of Chimeric Oligonucleotides

[0251] Chimeric oligonucleotides, oligonucleosides or mixed oligonucleotides/oligonucleosides of the invention can be of several different types. These include a first type wherein the “gap” segment of linked nucleosides is positioned between 5′ and 3′ “wing” segments of linked nucleosides and a second “open end” type wherein the “gap” segment is located at either the 3′ or the 5′ terminus of the oligomeric compound. Oligonucleotides of the first type are also known in the art as “gapmers” or gapped oligonucleotides. Oligonucleotides of the second type are also known in the art as “hemimers” or “wingmers”.

[0252] [2′-O-Me]--[2′-deoxy]--[2′-O-Me] Chimeric Phosphorothioate Oligonucleotides

[0253] Chimeric oligonucleotides having 2′-O-alkyl phosphorothioate and 2′-deoxy phosphorothioate oligo-nucleotide segments are synthesized using an Applied Biosystems automated DNA synthesizer Model 394, as above. Oligonucleotides are synthesized using the automated synthesizer and 2′-deoxy-5′-dimethoxytrityl-3′-O-phosphor-amidite for the DNA portion and 5′-dimethoxytrityl-2′-O-methyl-3′-O-phosphoramidite for 5′ and 3′ wings. The standard synthesis cycle is modified by incorporating coupling steps with increased reaction times for the 5′-dimethoxytrityl-2′-O-methyl-3′-O-phosphoramidite. The fully protected oligonucleotide is cleaved from the support and deprotected in concentrated ammonia (NH₄OH) for 12-16 hr at 552° C. The deprotected oligo is then recovered by an appropriate method (precipitation, column chromatography, volume reduced in vacuo and analyzed spetrophotometrically for yield and for purity by capillary electrophoresis and by mass spectrometry.

[0254] [2′-O-(2-Methoxyethyl)]-[2′-deoxy]-[2′-O-(Methoxyethyl)] Chimeric Phosphorothioate Oligonucleotides

[0255] [2′-O-(2-methoxyethyl)]-[2′-deoxy]-[-2′-O-(methoxyethyl)] chimeric phosphorothioate oligonucleotides were prepared as per the procedure above for the 2′-O-methyl chimeric oligonucleotide, with the substitution of 2′-O-(methoxyethyl) amidites for the 2′-O-methyl amidites.

[0256] [2′-O-(2-Methoxyethyl)Phosphodiester]-[2′-deoxy Phosphorothioate]-[2′-O-(2-Methoxyethyl) Phosphodiester] Chimeric Oligonucleotides

[0257] [2′-O-(2-methoxyethyl phosphodiester]-[2′-deoxy phosphorothioate]-[2′-O-(methoxyethyl) phosphodiester] chimeric oligonucleotides are prepared as per the above procedure for the 2′-O-methyl chimeric oligonucleotide with the substitution of 2′-O-(methoxyethyl) amidites for the 2′-O-methyl amidites, oxidation with iodine to generate the phosphodiester internucleotide linkages within the wing portions of the chimeric structures and sulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) to generate the phosphorothioate internucleotide linkages for the center gap.

[0258] Other chimeric oligonucleotides, chimeric oligonucleosides and mixed chimeric oligonucleotides/oligonucleosides are synthesized according to U.S. Pat. No. 5,623,065, herein incorporated by reference.

Example 6

[0259] Oligonucleotide Isolation

[0260] After cleavage from the controlled pore glass solid support and deblocking in concentrated ammonium hydroxide at 55° C. for 12-16 hours, the oligonucleotides or oligonucleosides are recovered by precipitation out of 1 M NH₄OAc with >3 volumes of ethanol. Synthesized oligonucleotides were analyzed by electrospray mass spectroscopy (molecular weight determination) and by capillary gel electrophoresis and judged to be at least 70% full length material. The relative amounts of phosphorothioate and phosphodiester linkages obtained in the synthesis was determined by the ratio of correct molecular weight relative to the −16 amu product (±32 ±48). For some studies oligonucleotides were purified by HPLC, as described by Chiang et al., J. Biol. Chem. 1991, 266, 18162-18171. Results obtained with HPLC-purified material were similar to those obtained with non-HPLC purified material.

Example 7

[0261] Oligonucleotide Synthesis-96 Well Plate Format

[0262] Oligonucleotides were synthesized via solid phase P(III) phosphoramidite chemistry on an automated synthesizer capable of assembling 96 sequences simultaneously in a 96-well format. Phosphodiester internucleotide linkages were afforded by oxidation with aqueous iodine. Phosphorothioate internucleotide linkages were generated by sulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) in anhydrous acetonitrile. Standard base-protected beta-cyanoethyl-diiso-propyl phosphoramidites were purchased from commercial vendors (e.g. PE-Applied Biosystems, Foster City, Calif., or Pharmacia, Piscataway, N.J.). Non-standard nucleosides are synthesized as per standard or patented methods. They are utilized as base protected beta-cyanoethyldiisopropyl phosphoramidites.

[0263] Oligonucleotides were cleaved from support and deprotected with concentrated NH₄OH at elevated temperature (55-60° C.) for 12-16 hours and the released product then dried in vacuo. The dried product was then re-suspended in sterile water to afford a master plate from which all analytical and test plate samples are then diluted utilizing robotic pipettors.

Example 8

[0264] Oligonucleotide Analysis—96-Well Plate Format

[0265] The concentration of oligonucleotide in each well was assessed by dilution of samples and UV absorption spectroscopy. The full-length integrity of the individual products was evaluated by capillary electrophoresis (CE) in either the 96-well format (Beckman P/ACE™ MDQ) or, for individually prepared samples, on a commercial CE apparatus (e.g., Beckman P/ACE™ 5000, ABI 270). Base and backbone composition was confirmed by mass analysis of the compounds utilizing electrospray-mass spectroscopy. All assay test plates were diluted from the master plate using single and multi-channel robotic pipettors. Plates were judged to be acceptable if at least 85% of the compounds on the plate were at least 85% full length.

Example 9

[0266] Cell Culture and Oligonucleotide Treatment

[0267] The effect of antisense compounds on target nucleic acid expression can be tested in any of a variety of cell types provided that the target nucleic acid is present at measurable levels. This can be routinely determined using, for example, PCR or Northern blot analysis. The following cell types are provided for illustrative purposes, but other cell types can be routinely used, provided that the target is expressed in the cell type chosen. This can be readily determined by methods routine in the art, for example Northern blot analysis, ribonuclease protection assays, or RT-PCR.

[0268] T-24 cells:

[0269] The human transitional cell bladder carcinoma cell line T-24 was obtained from the American Type Culture Collection (ATCC) (Manassas, Va.). T-24 cells were routinely cultured in complete McCoy's 5A basal media (Invitrogen Corporation, Carlsbad, Calif.) supplemented with 10% fetal calf serum (Invitrogen Corporation, Carlsbad, Calif.), penicillin 100 units per mL, and streptomycin 100 micrograms per mL (Invitrogen Corporation, Carlsbad, Calif.). Cells were routinely passaged by trypsinization and dilution when they reached 90% confluence. Cells were seeded into 96-well plates (Falcon-Primaria #3872) at a density of 7000 cells/well for use in RT-PCR analysis.

[0270] For Northern blotting or other analysis, cells may be seeded onto 100 mm or other standard tissue culture plates and treated similarly, using appropriate volumes of medium and oligonucleotide.

[0271] A549 cells:

[0272] The human lung carcinoma cell line A549 was obtained from the American Type Culture Collection (ATCC) (Manassas, Va.). A549 cells were routinely cultured in DMEM basal media (Invitrogen Corporation, Carlsbad, Calif.) supplemented with 10% fetal calf serum (Invitrogen Corporation, Carlsbad, Calif.), penicillin 100 units per mL, and streptomycin 100 micrograms per mL (Invitrogen Corporation, Carlsbad, Calif.). Cells were routinely passaged by trypsinization and dilution when they reached 90% confluence.

[0273] NHDF cells:

[0274] Human neonatal dermal fibroblast (NHDF) were obtained from the Clonetics Corporation (Walkersville, Md.). NHDFs were routinely maintained in Fibroblast Growth Medium (Clonetics Corporation, Walkersville, Md.) supplemented as recommended by the supplier. Cells were maintained for up to 10 passages as recommended by the supplier.

[0275] HEK cells:

[0276] Human embryonic keratinocytes (HEK) were obtained from the Clonetics Corporation (Walkersville, Md.). HEKs were routinely maintained in Keratinocyte Growth Medium (Clonetics Corporation, Walkersville, Md.) formulated as recommended by the supplier. Cells were routinely maintained for up to 10 passages as recommended by the supplier.

[0277] Treatment with antisense compounds:

[0278] When cells reached 70% confluency, they were treated with oligonucleotide. For cells grown in 96-well plates, wells were washed once with 100 μL OPTI-MEM™-1 reduced-serum medium (Invitrogen Corporation, Carlsbad, Calif.) and then treated with 130 μL of OPTI-MEM™-1 containing 3.75 μg/mL LIPOFECTIN™ (Invitrogen Corporation, Carlsbad, Calif.) and the desired concentration of oligonucleotide. After 4-7 hours of treatment, the medium was replaced with fresh medium. Cells were harvested 16-24 hours after oligonucleotide treatment.

[0279] The concentration of oligonucleotide used varies from cell line to cell line. To determine the optimal oligonucleotide concentration for a particular cell line, the cells are treated with a positive control oligonucleotide at a range of concentrations. For human cells the positive control oligonucleotide is selected from either ISIS 13920 (TCCGTCATCGCTCCTCAGGG, SEQ ID NO: 1) which is targeted to human H-ras, or ISIS 18078, (GTGCGCGCGAGCCCGAAATC, SEQ ID NO: 2) which is targeted to human Jun-N-terminal kinase-2 (JNK2). Both controls are 2′-O-methoxyethyl gapmers (2′-O-methoxyethyls shown in bold) with a phosphorothioate backbone. For mouse or rat cells the positive control oligonucleotide is ISIS 15770, ATGCATTCTGCCCCCAAGGA, SEQ ID NO: 3, a 2′-O-methoxyethyl gapmer (2′-O-methoxyethyls shown in bold) with a phosphorothioate backbone which is targeted to both mouse and rat c-raf. The concentration of positive control oligonucleotide that results in 80% inhibition of c-Ha-ras (for ISIS 13920) or c-raf (for ISIS 15770) mRNA is then utilized as the screening concentration for new oligonucleotides in subsequent experiments for that cell line. If 80% inhibition is not achieved, the lowest concentration of positive control oligonucleotide that results in 60% inhibition of H-ras or c-raf mRNA is then utilized as the oligonucleotide screening concentration in subsequent experiments for that cell line. If 60% inhibition is not achieved, that particular cell line is deemed as unsuitable for oligonucleotide transfection experiments. The concentrations of antisense oligonucleotides used herein are from 50 nM to 300 nM.

Example 10

[0280] Analysis of Oligonucleotide Inhibition of Breast Cancer-1 Expression

[0281] Antisense modulation of breast cancer-1 expression can be assayed in a variety of ways known in the art. For example, breast cancer-1 mRNA levels can be quantitated by, e.g., Northern blot analysis, competitive polymerase chain reaction (PCR), or real-time PCR (RT-PCR). Real-time quantitative PCR is presently preferred. RNA analysis can be performed on total cellular RNA or poly(A)+ mRNA. The preferred method of RNA analysis of the present invention is the use of total cellular RNA as described in other examples herein. Methods of RNA isolation are taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 1, pp. 4.1.1-4.2.9 and 4.5.1-4.5.3, John Wiley & Sons, Inc., 1993. Northern blot analysis is routine in the art and is taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 1, pp. 4.2.1-4.2.9, John Wiley & Sons, Inc., 1996. Real-time quantitative (PCR) can be conveniently accomplished using the commercially available ABI PRISM™ 7700 Sequence Detection System, available from PE-Applied Biosystems, Foster City, Calif. and used according to manufacturer's instructions.

[0282] Protein levels of breast cancer-1 can be quantitated in a variety of ways well known in the art, such as immunoprecipitation, Western blot analysis (immunoblotting), ELISA or fluorescence-activated cell sorting (FACS). Antibodies directed to breast cancer-1 can be identified and obtained from a variety of sources, such as the MSRS catalog of antibodies (Aerie Corporation, Birmingham, Mich.), or can be prepared via conventional antibody generation methods. Methods for preparation of polyclonal antisera are taught in, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 2, pp. 11.12.1-11.12.9, John Wiley & Sons, Inc., 1997). Preparation of monoclonal antibodies is taught in, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 2, pp. 11.4.1-11.11.5, John Wiley & Sons, Inc., 1997).

[0283] Immunoprecipitation methods are standard in the art and can be found at, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 2, pp. 10.16.1-10.16.11, John Wiley & Sons, Inc., 1998). Western blot (immunoblot) analysis is standard in the art and can be found at, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 2, pp. 10.8.1-10.8.21, John Wiley & Sons, Inc., 1997). Enzyme-linked-immunosorbent assays (ELISA) are standard in the art and can be found at, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 2, pp. 11.2.1-11.2.22, John Wiley & Sons, Inc., 1991).

Example 11

[0284] Poly(A)+ mRNA Isolation

[0285] Poly(A)+ mRNA was isolated according to Miura et al., (Clin. Chem., 1996, 42, 1758-1764). Other methods for poly(A)+ mRNA isolation are taught in, for example, Ausubel, F. M. et al., (Current Protocols in Molecular Biology, Volume 1, pp. 4.5.1-4.5.3, John Wiley & Sons, Inc., 1993). Briefly, for cells grown on 96-well plates, growth medium was removed from the cells and each well was washed with 200 μL cold PBS. 60 μL lysis buffer (10 mM Tris-HCl, pH 7.6, 1 mM EDTA, 0.5 M NaCl, 0.5% NP-40, 20 mM vanadyl-ribonucleoside complex) was added to each well, the plate was gently agitated and then incubated at room temperature for five minutes. 55 μL of lysate was transferred to Oligo d(T) coated 96-well plates (AGCT Inc., Irvine Calif.). Plates were incubated for 60 minutes at room temperature, washed 3 times with 200 μL of wash buffer (10 mM Tris-HCl pH 7.6, 1 mM EDTA, 0.3 M NaCl). After the final wash, the plate was blotted on paper towels to remove excess wash buffer and then air-dried for 5 minutes. 60 μL of elution buffer (5 mM Tris-HCl pH 7.6), preheated to 70° C., was added to each well, the plate was incubated on a 90° C. hot plate for 5 minutes, and the eluate was then transferred to a fresh 96-well plate.

[0286] Cells grown on 100 mm or other standard plates may be treated similarly, using appropriate volumes of all solutions.

Example 12

[0287] Total RNA Isolation

[0288] Total RNA was isolated using an RNEASY 96™ kit and buffers purchased from Qiagen Inc. (Valencia, Calif.) following the manufacturer's recommended procedures. Briefly, for cells grown on 96-well plates, growth medium was removed from the cells and each well was washed with 200 μL cold PBS. 150 μL Buffer RLT was added to each well and the plate vigorously agitated for 20 seconds. 150 μL of 70% ethanol was then added to each well and the contents mixed by pipetting three times up and down. The samples were then transferred to the RNEASY 96™ well plate attached to a QIAVAC™ manifold fitted with a waste collection tray and attached to a vacuum source. Vacuum was applied for 1 minute. 500 μL of Buffer RW1 was added to each well of the RNEASY 96™ plate and incubated for 15 minutes and the vacuum was again applied for 1 minute. An additional 500 μL of Buffer RW1 was added to each well of the RNEASY 96™ plate and the vacuum was applied for 2 minutes. 1 mL of Buffer RPE was then added to each well of the RNEASY 96™ plate and the vacuum applied for a period of 90 seconds. The Buffer RPE wash was then repeated and the vacuum was applied for an additional 3 minutes. The plate was then removed from the QIAVAC™ manifold and blotted dry on paper towels. The plate was then re-attached to the QIAVAC™ manifold fitted with a collection tube rack containing 1.2 mL collection tubes. RNA was then eluted by pipetting 170 μL water into each well, incubating 1 minute, and then applying the vacuum for 3 minutes.

[0289] The repetitive pipetting and elution steps may be automated using a QIAGEN Bio-Robot 9604 (Qiagen, Inc., Valencia Calif.). Essentially, after lysing of the cells on the culture plate, the plate is transferred to the robot deck where the pipetting, DNase treatment and elution steps are carried out.

Example 13

[0290] Real-Time Quantitative PCR Analysis of Breast Cancer-1 mRNA Levels

[0291] Quantitation of breast cancer-1 mRNA levels was determined by real-time quantitative PCR using the ABI PRISM™ 7700 Sequence Detection System (PE-Applied Biosystems, Foster City, Calif.) according to manufacturer's instructions. This is a closed-tube, non-gel-based, fluorescence detection system which allows high-throughput quantitation of polymerase chain reaction (PCR) products in real-time. As opposed to standard PCR in which amplification products are quantitated after the PCR is completed, products in real-time quantitative PCR are quantitated as they accumulate. This is accomplished by including in the PCR reaction an oligonucleotide probe that anneals specifically between the forward and reverse PCR primers, and contains two fluorescent dyes. A reporter dye (e.g., FAM or JOE, obtained from either PE-Applied Biosystems, Foster City, Calif., Operon Technologies Inc., Alameda, Calif. or Integrated DNA Technologies Inc., Coralville, Iowa) is attached to the 5′ end of the probe and a quencher dye (e.g., TAMRA, obtained from either PE-Applied Biosystems, Foster City, Calif., Operon Technologies Inc., Alameda, Calif. or Integrated DNA Technologies Inc., Coralville, Iowa) is attached to the 3′ end of the probe. When the probe and dyes are intact, reporter dye emission is quenched by the proximity of the 3′ quencher dye. During amplification, annealing of the probe to the target sequence creates a substrate that can be cleaved by the 5′-exonuclease activity of Taq polymerase. During the extension phase of the PCR amplification cycle, cleavage of the probe by Taq polymerase releases the reporter dye from the remainder of the probe (and hence from the quencher moiety) and a sequence-specific fluorescent signal is generated. With each cycle, additional reporter dye molecules are cleaved from their respective probes, and the fluorescence intensity is monitored at regular intervals by laser optics built into the ABI PRISM™ 7700 Sequence Detection System. In each assay, a series of parallel reactions containing serial dilutions of mRNA from untreated control samples generates a standard curve that is used to quantitate the percent inhibition after antisense oligonucleotide treatment of test samples.

[0292] Prior to quantitative PCR analysis, primer-probe sets specific to the target gene being measured are evaluated for their ability to be “multiplexed” with a GAPDH amplification reaction. In multiplexing, both the target gene and the internal standard gene GAPDH are amplified concurrently in a single sample. In this analysis, mRNA isolated from untreated cells is serially diluted. Each dilution is amplified in the presence of primer-probe sets specific for GAPDH only, target gene only (“single-plexing”), or both (multiplexing). Following PCR amplification, standard curves of GAPDH and target mRNA signal as a function of dilution are generated from both the single-plexed and multiplexed samples. If both the slope and correlation coefficient of the GAPDH and target signals generated from the multiplexed samples fall within 10% of their corresponding values generated from the single-plexed samples, the primer-probe set specific for that target is deemed multiplexable. Other methods of PCR are also known in the art.

[0293] PCR reagents were obtained from Invitrogen Corporation, (Carlsbad, Calif.). RT-PCR reactions were carried out by adding 20 μL PCR cocktail (2.5× PCR buffer (—MgCl2), 6.6 mM MgCl2, 375 μM each of DATP, dCTP, dCTP and dGTP, 375 nM each of forward primer and reverse primer, 125 nM of probe, 4 Units RNAse inhibitor, 1.25 Units PLATINUM® Taq, 5 Units MuLV reverse transcriptase, and 2.5× ROX dye) to 96-well plates containing 30 μL total RNA solution. The RT reaction was carried out by incubation for 30 minutes at 48° C. Following a 10 minute incubation at 95° C. to activate the PLATINUM® Taq, 40 cycles of a two-step PCR protocol were carried out: 95° C. for 15 seconds (denaturation) followed by 60° C. for 1.5 minutes (annealing/extension).

[0294] Gene target quantities obtained by real time RT-PCR are normalized using either the expression level of GAPDH, a gene whose expression is constant, or by quantifying total RNA using RiboGreen™ (Molecular Probes, Inc. Eugene, Oreg.). GAPDH expression is quantified by real time RT-PCR, by being run simultaneously with the target, multiplexing, or separately. Total RNA is quantified using RiboGreen™ RNA quantification reagent from Molecular Probes. Methods of RNA quantification by RiboGreen™ are taught in Jones, L. J., et al, (Analytical Biochemistry, 1998, 265, 368-374).

[0295] In this assay, 170 μL of RiboGreen™ working reagent (RiboGreen™ reagent diluted 1:350 in 10 mM Tris-HCl, 1 mM EDTA, pH 7.5) is pipetted into a 96-well plate containing 30 μL purified, cellular RNA. The plate is read in a CytoFluor 4000 (PE Applied Biosystems) with excitation at 480 nm and emission at 520 nm.

[0296] Probes and primers to human breast cancer-1 were designed to hybridize to a human breast cancer-1 sequence, using published sequence information (GenBank accession number U14680.1, incorporated herein as SEQ ID NO: 4). For human breast cancer-1 the PCR primers were: forward primer: TGCTCAGGGCTATCCTCTCAG (SEQ ID NO: 5) reverse primer: TGCTGGAGCTTTATCAGGTTATGT (SEQ ID NO: 6) and the PCR probe was: FAM-TGACATTTTAACCACTCAGCAGAGGGATACCA-TAMRA (SEQ ID NO: 7) where FAM is the fluorescent dye and TAMRA is the quencher dye. For human GAPDH the PCR primers were: forward primer: GAAGGTGAAGGTCGGAGTC(SEQ ID NO: 8) reverse primer: GAAGATGGTGATGGGATTTC (SEQ ID NO: 9) and the PCR probe was: 5′ JOE-CAAGCTTCCCGTTCTCAGCC-TAMRA 3′ (SEQ ID NO: 10) where JOE is the fluorescent reporter dye and TAMRA is the quencher dye.

Example 14

[0297] Northern Blot Analysis of Breast Cancer-1 mRNA Levels

[0298] Eighteen hours after antisense treatment, cell monolayers were washed twice with cold PBS and lysed in 1 mL RNAZOL™ (TEL-TEST “B” Inc., Friendswood, Tex.). Total RNA was prepared following manufacturer's recommended protocols. Twenty micrograms of total RNA was fractionated by electrophoresis through 1.2% agarose gels containing 1.1% formaldehyde using a MOPS buffer system (AMRESCO, Inc. Solon, Ohio). RNA was transferred from the gel to HYBOND™-N+ nylon membranes (Amersham Pharmacia Biotech, Piscataway, N.J.) by overnight capillary transfer using a Northern/Southern Transfer buffer system (TEL-TEST “B” Inc., Friendswood, Tex.). RNA transfer was confirmed by UV visualization. Membranes were fixed by UV cross-linking using a STRATALINKER™ UV Crosslinker 2400 (Stratagene, Inc, La Jolla, Calif.) and then probed using QUICKHYB™ hybridization solution (Stratagene, La Jolla, Calif.) using manufacturer's recommendations for stringent conditions.

[0299] To detect human breast cancer-1, a human breast cancer-1 specific probe was prepared by PCR using the forward primer TGCTCAGGGCTATCCTCTCAG (SEQ ID NO: 5) and the reverse primer TGCTGGAGCTTTATCAGGTTATGT (SEQ ID NO: 6). To normalize for variations in loading and transfer efficiency membranes were stripped and probed for human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) RNA (Clontech, Palo Alto, Calif.).

[0300] Hybridized membranes were visualized and quantitated using a PHOSPHORIMAGER™ and IMAGEQUANT™ Software V3.3 (Molecular Dynamics, Sunnyvale, Calif.). Data was normalized to GAPDH levels in untreated controls.

Example 15

[0301] Antisense Inhibition of Human Breast Cancer-1 Expression by Chimeric Phosphorothioate Oligonucleotides Having 2′-MOE Wings and a Deoxy Gap

[0302] In accordance with the present invention, a series of oligonucleotides were designed to target different regions of the human breast cancer-1 RNA, using published sequences (GenBank accession number U14680.1, incorporated herein as SEQ ID NO: 4, GenBank accession number NM_(—)007294.1, incorporated herein as SEQ ID NO: 11, GenBank accession number NM_(—)007295.1, incorporated herein as SEQ ID NO: 12, GenBank accession number NM_(—)007296.1, incorporated herein as SEQ ID NO: 13, GenBank accession number NM_(—)007297.1, incorporated herein as SEQ ID NO: 14, GenBank accession number NM_(—)007298.1, incorporated herein as SEQ ID NO: 15, GenBank accession number NM_(—)007299.1, incorporated herein as SEQ ID NO: 16, GenBank accession number NM_(—)007300.1, incorporated herein as SEQ ID NO: 17, GenBank accession number NM_(—)007301.1, incorporated herein as SEQ ID NO: 18, GenBank accession number NM_(—)007302.1, incorporated herein as SEQ ID NO: 19, GenBank accession number NM_(—)007303.1, incorporated herein as SEQ ID NO: 20, GenBank accession number NM_(—)007304.1, incorporated herein as SEQ ID NO: 21, GenBank accession number NM_(—)007306.1, incorporated herein as SEQ ID NO: 22, and nucleotide residues 150000-280000 of GenBank accession number NT_(—)010771.4, incorporated herein as SEQ ID NO: 23). The oligonucleotides are shown in Table 1. “Target site” indicates the first (5′-most) nucleotide number on the particular target sequence to which the oligonucleotide binds. All compounds in Table 1 are chimeric oligonucleotides (“gapmers”) 20 nucleotides in length, composed of a central “gap” region consisting of ten 2′-deoxynucleotides, which is flanked on both sides (5′ and 3′ directions) by five-nucleotide “wings”. The wings are composed of 2′-methoxyethyl (2′-MOE)nucleotides. The internucleoside (backbone) linkages are phosphorothioate (P═S) throughout the oligonucleotide. All cytidine residues are 5-methylcytidines. The compounds were analyzed for their effect on human breast cancer-1 mRNA levels by quantitative real-time PCR as described in other examples herein. Data are averages from two experiments. Oligonucleotides ISIS 159060-159162 of the present invention were used to treat T-24 cells and oligonucleotides 197030-197064 of the present invention were used to treat A549 cells. The positive control for each datapoint is identified in the table by sequence ID number. The positive control for each datapoint is identified in the table by sequence ID number. If present, “N.D.” indicates “no data”. TABLE 1 Inhibition of human breast cancer-1 mRNA levels by chimeric phosphorothioate oligonucleotides having 2′-MOE wings and a deoxy gap TARGET SEQ ID TARGET SEQ CONTROL ISIS # REGION NO SITE SEQUENCE % INHIB ID NO SEQ ID NO 159060 Coding 4 4663 gtttctattctgaagactcc 61 24 2 159062 Coding 4 1182 gagcatggcagtttctgctt 59 25 2 159065 Coding 4 487 gcccatactttggatgatag 72 26 2 159067 Coding 4 2916 actggcttatctttctgacc 83 27 2 159069 Coding 4 3470 aatctgtattaacagtctga 61 28 2 159071 Coding 4 5061 accaccatggacattctttt 51 29 2 159074 Coding 4 3788 acaagtgttggaagcaggga 39 30 2 159077 Coding 4 3036 cgatatgggttttgtaaaag 36 31 2 159080 Coding 4 2945 ctcotttgatactacatttg 34 32 2 159083 Coding 4 509 gtcttttggcacggtttctg 65 33 2 159087 Coding 4 2213 catttgttaacttcagctct 38 34 2 159090 Coding 4 941 tggcatgagtatttgtgcca 49 35 2 159092 Coding 4 798 acatccgtctcagaaaattc 68 36 2 159096 Coding 4 1566 tcagtaacaaatgctcctat 71 37 2 159098 Coding 4 4279 ggttaaaatgtcactctgag 47 38 2 159102 Coding 4 355 ctcttcaacaagttgactaa 67 39 2 159104 Coding 4 3730 ctctaatttcttggcccctc 57 40 2 159107 Coding 4 1497 cgataggttttcccaaatat 57 41 2 159110 Coding 4 1514 ggaggcttgccttcttccga 59 42 2 159113 Coding 4 5664 atcaggtaggtgtccagctc 64 43 2 159116 Coding 4 3369 tgcaaaacccctaatctaag 71 44 2 159119 Coding 4 3934 ctttgccaatattacctggt 56 45 2 159122 Coding 4 5163 acaacatgagtagtctcttc 59 46 2 159125 Coding 4 5583 cacatctgcccaattgcatg 52 47 2 159128 Coding 4 4334 ccatttcctgctggagcttt 34 48 2 159131 Coding 4 4360 ctgttctaacacagcttcta 31 49 2 159134 Coding 4 3185 tacggctaattgtgctcact 73 50 2 159137 Coding 4 2608 ttcatgtcccaatggatact 60 51 2 159140 Coding 4 3640 gcttttgctaaaaacagcag 47 52 2 159141 Coding 4 447 tcaggagagttattttcctt 64 53 2 159144 Coding 4 4414 ggcagaagagtcacttatga 55 54 2 159147 Coding 4 1045 ccttgctaagccaggctgtt 55 55 2 159150 Coding 4 5224 cgcaattcctagaaaatatt 44 56 2 159153 Coding 4 4957 agtatgagcagcagctggac 59 57 2 159156 Coding 4 3733 ggactctaatttcttggccc 86 58 2 159159 Coding 4 4760 gcaagtaagatgtttccgtc 50 59 2 159162 Coding 4 2023 aatttgcaattcagtacaat 53 60 2 197030 Start 4 112 agataaatccatttctttct 58 61 2 Codon 197031 Coding 4 5387 ccctgaagatctttctgtcc 65 62 2 197032 3′ UTR 11 5842 tacataaaatatttagtagc 26 63 2 197033 3′ UTR 11 6099 gggaaaccagctattctctt 73 64 2 197034 3′ UTR 11 6460 gtagctgggattacaggtgt 82 65 2 197035 3′ UTR 11 6785 ccagaggtcttatattttaa 84 66 2 197036 3′ UTR 11 6790 tcatgccagaggtcttatat 73 67 2 197037 3′ UTR 11 6824 tggtgggatctgtcatttta 63 68 2 197038 3′ UTR 11 6929 actttttcttccttcagcaa 65 69 2 197039 3′ UTR 11 7081 accaagtttatttgcagtgt 70 70 2 197040 5′ UTR 12 49 attcccccacggacactcag 50 71 2 197041 5′ UTR 12 195 acgcccggctaatttttgta 60 72 2 197042 5′ UTR 12 307 ctctgtcgcccaggctggag 70 73 2 197043 5′ UTR 12 369 ttccaatgaacagccggtgt 40 74 2 197044 5′ UTR 13 107 ttccaatgaaccagagcaga 36 75 2 197045 5′ UTR 14 113 tcacaagcagctttacccag 19 76 2 197046 Coding 15 679 gctgcttcacccaattcaat 50 77 2 197047 Coding 16 4489 aactcagcatctttttctga 21 78 2 197048 Coding 17 4489 tgggtcacccctttttctga 0 79 2 197049 Stop 18 4616 aactcagcatctttccactc 3 80 2 Codon 197050 Coding 19 679 tcacaagcagccaattcaat 35 81 2 197051 Coding 20 805 gatgctgcttcacccttttt 66 82 2 197052 Coding 21 919 gctgcttcaccctgatactt 53 83 2 197053 Coding 21 1080 tcccatgctgttctaacaca 37 84 2 197054 Coding 22 266 gagtaagaccttgcaaaata 12 85 2 197055 3′ UTR 22 382 catgcaaaatagtcccagct 40 86 2 197056 exon: 23 12111 actctactacctttacccag 25 87 2 intron junction 197057 exon: 23 12645 tcatacataccagccggtgt 80 88 2 intron junction 197058 intron: 23 26800 gagtaagaccctgtctcaaa 49 89 2 exon junction 197059 exon: 23 26916 gtgcacttacagtcccagct 58 90 2 intron junction 197060 exon: 23 42635 acagaactaccctgatactt 62 91 2 intron junction 197061 intron: 23 60764 gttaatactgctttaaatgg 19 92 2 exon junction 197062 intron 23 84117 ttctccccaggcagccaagt 66 93 2 197063 exon: 23 86321 aggctcttacctgtgggcat 48 94 2 intron junction 197064 intron 23 87482 tctgtctgactgaacgaagg 60 95 2

[0303] As shown in Table 1, SEQ ID NOs 24, 25, 26, 27, 28, 29, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 50, 51, 52, 53, 54, 55, 57, 58, 59, 60, 61, 62, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 77, 82, 83, 88, 89, 90, 91, 93, 94 and 95 demonstrated at least 47% inhibition of human breast cancer-1 expression in this assay and are therefore preferred. The target sites to which these preferred sequences are complementary are herein referred to as “preferred target regions” and are therefore preferred sites for targeting by compounds of the present invention. These preferred target regions are shown in Table 2. The sequences represent the reverse complement of the preferred antisense compounds shown in Table 1. “Target site” indicates the first (5′-most) nucleotide number of the corresponding target nucleic acid. Also shown in Table 2 is the species in which each of the preferred target regions was found. TABLE 2 Sequence and position of preferred target regions identified in breast cancer-1. REV COMP SITE TARGET TARGET OF SEQ SEQ ID ID SEQ ID NO SITE SEQUENCE ID ACTIVE IN NO 74361 4 4663 ggagtcttcagaatagaaac 24 H. sapiens 96 74362 4 1182 aagoagaaactgccatgctc 25 H. sapiens 97 74363 4 487 ctatcatccaaagtatgggc 26 H. sapiens 98 74364 4 2916 ggtcagaaagataagccagt 27 H. sapiens 99 74365 4 3470 tcagactgttaatacagatt 28 H. sapiens 100 74366 4 5061 aaaagaatgtccatggtggt 29 H. sapiens 101 74370 4 509 cagaaaccgtgccaaaagac 33 H. sapiens 102 74372 4 941 tggcacaaatactcatgcca 35 H. sapiens 103 74373 4 798 gaattttctgagacggatgt 36 H. sapiens 104 74374 4 1566 ataggagcatttgttactga 37 H. sapiens 105 74375 4 4279 ctcagagtgacattttaacc 38 H. sapiens 106 74376 4 355 ttagtcaacttgttgaagag 39 H. sapiens 107 74377 4 3730 gaggggccaagaaattagag 40 H. sapiens 108 74378 4 1497 atatttgggaaaacctatcg 41 H. sapiens 109 74379 4 1514 tcggaagaaggcaagcctcc 42 H. sapiens 110 74380 4 5664 gagctggacacctacctgat 43 H. sapiens 111 74381 4 3369 cttagattaggggttttgca 44 H. sapiens 112 74382 4 3934 accaggtaatattggcaaag 45 H. sapiens 113 74383 4 5163 gaagagactactcatgttgt 46 H. sapiens 114 74384 4 5583 catgcaattgggcagatgtg 47 H. sapiens 115 74387 4 3185 agtgagcacaattagccgta 50 H. sapiens 116 74388 4 2608 agtatccattgggacatgaa 51 H. sapiens 117 74389 4 3640 ctgctgtttttageaaaagc 52 H. sapiens 118 74390 4 447 aaggaaaataactctcctga 53 H. sapiens 119 74391 4 4414 tcataagtgactcttctgcc 54 H. sapiens 120 74392 4 1045 aacagcctggcttagcaagg 55 H. sapiens 121 74394 4 4957 gtccagctgctgctcatact 57 H. sapiens 122 74395 4 3733 gggccaagaaattagagtcc 58 H. sapiens 123 74396 4 4760 gacggaaacatcttacttgc 59 H. sapiens 124 74397 4 2023 attgtactgaattgcaaatt 60 H. sapiens 125 115122 4 112 agaaagaaatggatttatct 61 H. sapiens 126 115123 4 5387 ggacagaaagatcttcaggg 62 H. sapiens 127 115125 11 6099 aagagaatagctggtttccc 64 H. sapiens 128 115126 11 6460 acacctgtaatcccagctac 65 H. sapiens 129 115127 11 6785 ttaaaatataagacctctgg 66 H. sapiens 130 115128 11 6790 atataagacctctggcatga 67 H. sapiens 131 115129 11 6824 taaaatgacagatcccacca 68 H. sapiens 132 115130 11 6929 ttgctgaaggaagaaaaagt 69 H. sapiens 133 115131 11 7081 acactgcaaataaacttggt 70 H. sapiens 134 115132 12 49 ctgagtgtccgtgggggaat 71 H. sapiens 135 115133 12 195 tacaaaaattagccgggcgt 72 H. sapiens 136 115134 12 307 ctccagcctgggcgacagag 73 H. sapiens 137 115138 15 679 attgaattgggtgaagcagc 77 H. sapiens 138 115143 20 805 aaaaagggtgaagcagcatc 82 H. sapiens 139 115144 21 919 aagtatcagggtgaagcagc 83 H. sapiens 140 115149 23 12645 acaccggctggtatgtatga 88 H. sapiens 141 115150 23 26800 tttgagacagggtcttactc 89 H. sapiens 142 115151 23 26916 agctgggactgtaagtgcac 90 H. sapiens 143 115152 23 42635 aagtatcagggtagttctgt 91 H. sapiens 144 115154 23 84117 acttggctgcctggggagaa 93 H. sapiens 145 115155 23 86321 atgcccacaggtaagagcct 94 H. sapiens 146 115156 23 87482 ccttcgttcagtcagacaga 95 H. sapiens 147

[0304] As these “preferred target regions” have been found by experimentation to be open to, and accessible for, hybridization with the antisense compounds of the present invention, one of skill in the art will recognize or be able to ascertain, using no more than routine experimentation, further embodiments of the invention that encompass other compounds that specifically hybridize to these sites and consequently inhibit the expression of breast cancer-1.

[0305] In one embodiment, the “preferred target region” may be employed in screening candidate antisense compounds. “Candidate antisense compounds” are those that inhibit the expression of a nucleic acid molecule encoding breast cancer-1 and which comprise at least an 8-nucleobase portion which is complementary to a preferred target region. The method comprises the steps of contacting a preferred target region of a nucleic acid molecule encoding breast cancer-1 with one or more candidate antisense compounds, and selecting for one or more candidate antisense compounds which inhibit the expression of a nucleic acid molecule encoding breast cancer-1. Once it is shown that the candidate antisense compound or compounds are capable of inhibiting the expression of a nucleic acid molecule encoding breast cancer-1, the candidate antisense compound may be employed as an antisense compound in accordance with the present invention.

[0306] According to the present invention, antisense compounds include ribozymes, external guide sequence (EGS) oligonucleotides (oligozymes), and other short catalytic RNAs or catalytic oligonucleotides which hybridize to the target nucleic acid and modulate its expression.

Example 16

[0307] Western Blot Analysis of Breast Cancer-1 Protein Levels

[0308] Western blot analysis (immunoblot analysis) is carried out using standard methods. Cells are harvested 16-20 h after oligonucleotide treatment, washed once with PBS, suspended in Laemmli buffer (100 ul/well), boiled for 5 minutes and loaded on a 16% SDS-PAGE gel. Gels are run for 1.5 hours at 150 V, and transferred to membrane for western blotting. Appropriate primary antibody directed to breast cancer-1 is used, with a radiolabeled or fluorescently labeled secondary antibody directed against the primary antibody species. Bands are visualized using a PHOSPHORIMAGER™ (Molecular Dynamics, Sunnyvale Calif.).

1 84 1 20 DNA Artificial Sequence Antisense Oligonucleotide 1 tccgtcatcg ctcctcaggg 20 2 20 DNA Artificial Sequence Antisense Oligonucleotide 2 gtgcgcgcga gcccgaaatc 20 3 20 DNA Artificial Sequence Antisense Oligonucleotide 3 atgcattctg cccccaagga 20 4 5711 DNA H. sapiens CDS (120)...(5711) 4 agctcgctga gacttcctgg accccgcacc aggctgtggg gtttctcaga taactgggcc 60 cctgcgctca ggaggccttc accctctgct ctgggtaaag ttcattggaa cagaaagaa 119 atg gat tta tct gct ctt cgc gtt gaa gaa gta caa aat gtc att aat 167 Met Asp Leu Ser Ala Leu Arg Val Glu Glu Val Gln Asn Val Ile Asn 1 5 10 15 gct atg cag aaa atc tta gag tgt ccc atc tgt ctg gag ttg atc aag 215 Ala Met Gln Lys Ile Leu Glu Cys Pro Ile Cys Leu Glu Leu Ile Lys 20 25 30 gaa cct gtc tcc aca aag tgt gac cac ata ttt tgc aaa ttt tgc atg 263 Glu Pro Val Ser Thr Lys Cys Asp His Ile Phe Cys Lys Phe Cys Met 35 40 45 ctg aaa ctt ctc aac cag aag aaa ggg cct tca cag tgt cct tta tgt 311 Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro Ser Gln Cys Pro Leu Cys 50 55 60 aag aat gat ata acc aaa agg agc cta caa gaa agt acg aga ttt agt 359 Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln Glu Ser Thr Arg Phe Ser 65 70 75 80 caa ctt gtt gaa gag cta ttg aaa atc att tgt gct ttt cag ctt gac 407 Gln Leu Val Glu Glu Leu Leu Lys Ile Ile Cys Ala Phe Gln Leu Asp 85 90 95 aca ggt ttg gag tat gca aac agc tat aat ttt gca aaa aag gaa aat 455 Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn Phe Ala Lys Lys Glu Asn 100 105 110 aac tct cct gaa cat cta aaa gat gaa gtt tct atc atc caa agt atg 503 Asn Ser Pro Glu His Leu Lys Asp Glu Val Ser Ile Ile Gln Ser Met 115 120 125 ggc tac aga aac cgt gcc aaa aga ctt cta cag agt gaa ccc gaa aat 551 Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu Gln Ser Glu Pro Glu Asn 130 135 140 cct tcc ttg cag gaa acc agt ctc agt gtc caa ctc tct aac ctt gga 599 Pro Ser Leu Gln Glu Thr Ser Leu Ser Val Gln Leu Ser Asn Leu Gly 145 150 155 160 act gtg aga act ctg agg aca aag cag cgg ata caa cct caa aag acg 647 Thr Val Arg Thr Leu Arg Thr Lys Gln Arg Ile Gln Pro Gln Lys Thr 165 170 175 tct gtc tac att gaa ttg gga tct gat tct tct gaa gat acc gtt aat 695 Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser Ser Glu Asp Thr Val Asn 180 185 190 aag gca act tat tgc agt gtg gga gat caa gaa ttg tta caa atc acc 743 Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln Glu Leu Leu Gln Ile Thr 195 200 205 cct caa gga acc agg gat gaa atc agt ttg gat tct gca aaa aag gct 791 Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu Asp Ser Ala Lys Lys Ala 210 215 220 gct tgt gaa ttt tct gag acg gat gta aca aat act gaa cat cat caa 839 Ala Cys Glu Phe Ser Glu Thr Asp Val Thr Asn Thr Glu His His Gln 225 230 235 240 ccc agt aat aat gat ttg aac acc act gag aag cgt gca gct gag agg 887 Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu Lys Arg Ala Ala Glu Arg 245 250 255 cat cca gaa aag tat cag ggt agt tct gtt tca aac ttg cat gtg gag 935 His Pro Glu Lys Tyr Gln Gly Ser Ser Val Ser Asn Leu His Val Glu 260 265 270 cca tgt ggc aca aat act cat gcc agc tca tta cag cat gag aac agc 983 Pro Cys Gly Thr Asn Thr His Ala Ser Ser Leu Gln His Glu Asn Ser 275 280 285 agt tta tta ctc act aaa gac aga atg aat gta gaa aag gct gaa ttc 1031 Ser Leu Leu Leu Thr Lys Asp Arg Met Asn Val Glu Lys Ala Glu Phe 290 295 300 tgt aat aaa agc aaa cag cct ggc tta gca agg agc caa cat aac aga 1079 Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala Arg Ser Gln His Asn Arg 305 310 315 320 tgg gct gga agt aag gaa aca tgt aat gat agg cgg act ccc agc aca 1127 Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp Arg Arg Thr Pro Ser Thr 325 330 335 gaa aaa aag gta gat ctg aat gct gat ccc ctg tgt gag aga aaa gaa 1175 Glu Lys Lys Val Asp Leu Asn Ala Asp Pro Leu Cys Glu Arg Lys Glu 340 345 350 tgg aat aag cag aaa ctg cca tgc tca gag aat cct aga gat act gaa 1223 Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu Asn Pro Arg Asp Thr Glu 355 360 365 gat gtt cct tgg ata aca cta aat agc agc att cag aaa gtt aat gag 1271 Asp Val Pro Trp Ile Thr Leu Asn Ser Ser Ile Gln Lys Val Asn Glu 370 375 380 tgg ttt tcc aga agt gat gaa ctg tta ggt tct gat gac tca cat gat 1319 Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly Ser Asp Asp Ser His Asp 385 390 395 400 ggg gag tct gaa tca aat gcc aaa gta gct gat gta ttg gac gtt cta 1367 Gly Glu Ser Glu Ser Asn Ala Lys Val Ala Asp Val Leu Asp Val Leu 405 410 415 aat gag gta gat gaa tat tct ggt tct tca gag aaa ata gac tta ctg 1415 Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser Glu Lys Ile Asp Leu Leu 420 425 430 gcc agt gat cct cat gag gct tta ata tgt aaa agt gaa aga gtt cac 1463 Ala Ser Asp Pro His Glu Ala Leu Ile Cys Lys Ser Glu Arg Val His 435 440 445 tcc aaa tca gta gag agt aat att gaa gac aaa ata ttt ggg aaa acc 1511 Ser Lys Ser Val Glu Ser Asn Ile Glu Asp Lys Ile Phe Gly Lys Thr 450 455 460 tat cgg aag aag gca agc ctc ccc aac tta agc cat gta act gaa aat 1559 Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu Ser His Val Thr Glu Asn 465 470 475 480 cta att ata gga gca ttt gtt act gag cca cag ata ata caa gag cgt 1607 Leu Ile Ile Gly Ala Phe Val Thr Glu Pro Gln Ile Ile Gln Glu Arg 485 490 495 ccc ctc aca aat aaa tta aag cgt aaa agg aga cct aca tca ggc ctt 1655 Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg Arg Pro Thr Ser Gly Leu 500 505 510 cat cct gag gat ttt atc aag aaa gca gat ttg gca gtt caa aag act 1703 His Pro Glu Asp Phe Ile Lys Lys Ala Asp Leu Ala Val Gln Lys Thr 515 520 525 cct gaa atg ata aat cag gga act aac caa acg gag cag aat ggt caa 1751 Pro Glu Met Ile Asn Gln Gly Thr Asn Gln Thr Glu Gln Asn Gly Gln 530 535 540 gtg atg aat att act aat agt ggt cat gag aat aaa aca aaa ggt gat 1799 Val Met Asn Ile Thr Asn Ser Gly His Glu Asn Lys Thr Lys Gly Asp 545 550 555 560 tct att cag aat gag aaa aat cct aac cca ata gaa tca ctc gaa aaa 1847 Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro Ile Glu Ser Leu Glu Lys 565 570 575 gaa tct gct ttc aaa acg aaa gct gaa cct ata agc agc agt ata agc 1895 Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro Ile Ser Ser Ser Ile Ser 580 585 590 aat atg gaa ctc gaa tta aat atc cac aat tca aaa gca cct aaa aag 1943 Asn Met Glu Leu Glu Leu Asn Ile His Asn Ser Lys Ala Pro Lys Lys 595 600 605 aat agg ctg agg agg aag tct tct acc agg cat att cat gcg ctt gaa 1991 Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg His Ile His Ala Leu Glu 610 615 620 cta gta gtc agt aga aat cta agc cca cct aat tgt act gaa ttg caa 2039 Leu Val Val Ser Arg Asn Leu Ser Pro Pro Asn Cys Thr Glu Leu Gln 625 630 635 640 att gat agt tgt tct agc agt gaa gag ata aag aaa aaa aag tac aac 2087 Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile Lys Lys Lys Lys Tyr Asn 645 650 655 caa atg cca gtc agg cac agc aga aac cta caa ctc atg gaa ggt aaa 2135 Gln Met Pro Val Arg His Ser Arg Asn Leu Gln Leu Met Glu Gly Lys 660 665 670 gaa cct gca act gga gcc aag aag agt aac aag cca aat gaa cag aca 2183 Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn Lys Pro Asn Glu Gln Thr 675 680 685 agt aaa aga cat gac agc gat act ttc cca gag ctg aag tta aca aat 2231 Ser Lys Arg His Asp Ser Asp Thr Phe Pro Glu Leu Lys Leu Thr Asn 690 695 700 gca cct ggt tct ttt act aag tgt tca aat acc agt gaa ctt aaa gaa 2279 Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn Thr Ser Glu Leu Lys Glu 705 710 715 720 ttt gtc aat cct agc ctt cca aga gaa gaa aaa gaa gag aaa cta gaa 2327 Phe Val Asn Pro Ser Leu Pro Arg Glu Glu Lys Glu Glu Lys Leu Glu 725 730 735 aca gtt aaa gtg tct aat aat gct gaa gac ccc aaa gat ctc atg tta 2375 Thr Val Lys Val Ser Asn Asn Ala Glu Asp Pro Lys Asp Leu Met Leu 740 745 750 agt gga gaa agg gtt ttg caa act gaa aga tct gta gag agt agc agt 2423 Ser Gly Glu Arg Val Leu Gln Thr Glu Arg Ser Val Glu Ser Ser Ser 755 760 765 att tca ttg gta cct ggt act gat tat ggc act cag gaa agt atc tcg 2471 Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly Thr Gln Glu Ser Ile Ser 770 775 780 tta ctg gaa gtt agc act cta ggg aag gca aaa aca gaa cca aat aaa 2519 Leu Leu Glu Val Ser Thr Leu Gly Lys Ala Lys Thr Glu Pro Asn Lys 785 790 795 800 tgt gtg agt cag tgt gca gca ttt gaa aac ccc aag gga cta att cat 2567 Cys Val Ser Gln Cys Ala Ala Phe Glu Asn Pro Lys Gly Leu Ile His 805 810 815 ggt tgt tcc aaa gat aat aga aat gac aca gaa ggc ttt aag tat cca 2615 Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr Glu Gly Phe Lys Tyr Pro 820 825 830 ttg gga cat gaa gtt aac cac agt cgg gaa aca agc ata gaa atg gaa 2663 Leu Gly His Glu Val Asn His Ser Arg Glu Thr Ser Ile Glu Met Glu 835 840 845 gaa agt gaa ctt gat gct cag tat ttg cag aat aca ttc aag gtt tca 2711 Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln Asn Thr Phe Lys Val Ser 850 855 860 aag cgc cag tca ttt gct ccg ttt tca aat cca gga aat gca gaa gag 2759 Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn Pro Gly Asn Ala Glu Glu 865 870 875 880 gaa tgt gca aca ttc tct gcc cac tct ggg tcc tta aag aaa caa agt 2807 Glu Cys Ala Thr Phe Ser Ala His Ser Gly Ser Leu Lys Lys Gln Ser 885 890 895 cca aaa gtc act ttt gaa tgt gaa caa aag gaa gaa aat caa gga aag 2855 Pro Lys Val Thr Phe Glu Cys Glu Gln Lys Glu Glu Asn Gln Gly Lys 900 905 910 aat gag tct aat atc aag cct gta cag aca gtt aat atc act gca ggc 2903 Asn Glu Ser Asn Ile Lys Pro Val Gln Thr Val Asn Ile Thr Ala Gly 915 920 925 ttt cct gtg gtt ggt cag aaa gat aag cca gtt gat aat gcc aaa tgt 2951 Phe Pro Val Val Gly Gln Lys Asp Lys Pro Val Asp Asn Ala Lys Cys 930 935 940 agt atc aaa gga ggc tct agg ttt tgt cta tca tct cag ttc aga ggc 2999 Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu Ser Ser Gln Phe Arg Gly 945 950 955 960 aac gaa act gga ctc att act cca aat aaa cat gga ctt tta caa aac 3047 Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys His Gly Leu Leu Gln Asn 965 970 975 cca tat cgt ata cca cca ctt ttt ccc atc aag tca ttt gtt aaa act 3095 Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile Lys Ser Phe Val Lys Thr 980 985 990 aaa tgt aag aaa aat ctg cta gag gaa aac ttt gag gaa cat tca atg 3143 Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn Phe Glu Glu His Ser Met 995 1000 1005 tca cct gaa aga gaa atg gga aat gag aac att cca agt aca gtg agc 3191 Ser Pro Glu Arg Glu Met Gly Asn Glu Asn Ile Pro Ser Thr Val Ser 1010 1015 1020 aca att agc cgt aat aac att aga gaa aat gtt ttt aaa gaa gcc agc 3239 Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn Val Phe Lys Glu Ala Ser 1025 1030 1035 1040 tca agc aat att aat gaa gta ggt tcc agt act aat gaa gtg ggc tcc 3287 Ser Ser Asn Ile Asn Glu Val Gly Ser Ser Thr Asn Glu Val Gly Ser 1045 1050 1055 agt att aat gaa ata ggt tcc agt gat gaa aac att caa gca gaa cta 3335 Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu Asn Ile Gln Ala Glu Leu 1060 1065 1070 ggt aga aac aga ggg cca aaa ttg aat gct atg ctt aga tta ggg gtt 3383 Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala Met Leu Arg Leu Gly Val 1075 1080 1085 ttg caa cct gag gtc tat aaa caa agt ctt cct gga agt aat tgt aag 3431 Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu Pro Gly Ser Asn Cys Lys 1090 1095 1100 cat cct gaa ata aaa aag caa gaa tat gaa gaa gta gtt cag act gtt 3479 His Pro Glu Ile Lys Lys Gln Glu Tyr Glu Glu Val Val Gln Thr Val 1105 1110 1115 1120 aat aca gat ttc tct cca tat ctg att tca gat aac tta gaa cag cct 3527 Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser Asp Asn Leu Glu Gln Pro 1125 1130 1135 atg gga agt agt cat gca tct cag gtt tgt tct gag aca cct gat gac 3575 Met Gly Ser Ser His Ala Ser Gln Val Cys Ser Glu Thr Pro Asp Asp 1140 1145 1150 ctg tta gat gat ggt gaa ata aag gaa gat act agt ttt gct gaa aat 3623 Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp Thr Ser Phe Ala Glu Asn 1155 1160 1165 gac att aag gaa agt tct gct gtt ttt agc aaa agc gtc cag aaa gga 3671 Asp Ile Lys Glu Ser Ser Ala Val Phe Ser Lys Ser Val Gln Lys Gly 1170 1175 1180 gag ctt agc agg agt cct agc cct ttc acc cat aca cat ttg gct cag 3719 Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr His Thr His Leu Ala Gln 1185 1190 1195 1200 ggt tac cga aga ggg gcc aag aaa tta gag tcc tca gaa gag aac tta 3767 Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu Ser Ser Glu Glu Asn Leu 1205 1210 1215 tct agt gag gat gaa gag ctt ccc tgc ttc caa cac ttg tta ttt ggt 3815 Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe Gln His Leu Leu Phe Gly 1220 1225 1230 aaa gta aac aat ata cct tct cag tct act agg cat agc acc gtt gct 3863 Lys Val Asn Asn Ile Pro Ser Gln Ser Thr Arg His Ser Thr Val Ala 1235 1240 1245 acc gag tgt ctg tct aag aac aca gag gag aat tta tta tca ttg aag 3911 Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu Asn Leu Leu Ser Leu Lys 1250 1255 1260 aat agc tta aat gac tgc agt aac cag gta ata ttg gca aag gca tct 3959 Asn Ser Leu Asn Asp Cys Ser Asn Gln Val Ile Leu Ala Lys Ala Ser 1265 1270 1275 1280 cag gaa cat cac ctt agt gag gaa aca aaa tgt tct gct agc ttg ttt 4007 Gln Glu His His Leu Ser Glu Glu Thr Lys Cys Ser Ala Ser Leu Phe 1285 1290 1295 tct tca cag tgc agt gaa ttg gaa gac ttg act gca aat aca aac acc 4055 Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu Thr Ala Asn Thr Asn Thr 1300 1305 1310 cag gat cct ttc ttg att ggt tct tcc aaa caa atg agg cat cag tct 4103 Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys Gln Met Arg His Gln Ser 1315 1320 1325 gaa agc cag gga gtt ggt ctg agt gac aag gaa ttg gtt tca gat gat 4151 Glu Ser Gln Gly Val Gly Leu Ser Asp Lys Glu Leu Val Ser Asp Asp 1330 1335 1340 gaa gaa aga gga acg ggc ttg gaa gaa aat aat caa gaa gag caa agc 4199 Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn Asn Gln Glu Glu Gln Ser 1345 1350 1355 1360 atg gat tca aac tta ggt gaa gca gca tct ggg tgt gag agt gaa aca 4247 Met Asp Ser Asn Leu Gly Glu Ala Ala Ser Gly Cys Glu Ser Glu Thr 1365 1370 1375 agc gtc tct gaa gac tgc tca ggg cta tcc tct cag agt gac att tta 4295 Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Ser Gln Ser Asp Ile Leu 1380 1385 1390 acc act cag cag agg gat acc atg caa cat aac ctg ata aag ctc cag 4343 Thr Thr Gln Gln Arg Asp Thr Met Gln His Asn Leu Ile Lys Leu Gln 1395 1400 1405 cag gaa atg gct gaa cta gaa gct gtg tta gaa cag cat ggg agc cag 4391 Gln Glu Met Ala Glu Leu Glu Ala Val Leu Glu Gln His Gly Ser Gln 1410 1415 1420 cct tct aac agc tac cct tcc atc ata agt gac tct tct gcc ctt gag 4439 Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser Asp Ser Ser Ala Leu Glu 1425 1430 1435 1440 gac ctg cga aat cca gaa caa agc aca tca gaa aaa gca gta tta act 4487 Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Glu Lys Ala Val Leu Thr 1445 1450 1455 tca cag aaa agt agt gaa tac cct ata agc cag aat cca gaa ggc ctt 4535 Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gln Asn Pro Glu Gly Leu 1460 1465 1470 tct gct gac aag ttt gag gtg tct gca gat agt tct acc agt aaa aat 4583 Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Ser Ser Thr Ser Lys Asn 1475 1480 1485 aaa gaa cca gga gtg gaa agg tca tcc cct tct aaa tgc cca tca tta 4631 Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Ser Lys Cys Pro Ser Leu 1490 1495 1500 gat gat agg tgg tac atg cac agt tgc tct ggg agt ctt cag aat aga 4679 Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gly Ser Leu Gln Asn Arg 1505 1510 1515 1520 aac tac cca tct caa gag gag ctc att aag gtt gtt gat gtg gag gag 4727 Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys Val Val Asp Val Glu Glu 1525 1530 1535 caa cag ctg gaa gag tct ggg cca cac gat ttg acg gaa aca tct tac 4775 Gln Gln Leu Glu Glu Ser Gly Pro His Asp Leu Thr Glu Thr Ser Tyr 1540 1545 1550 ttg cca agg caa gat cta gag gga acc cct tac ctg gaa tct gga atc 4823 Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Tyr Leu Glu Ser Gly Ile 1555 1560 1565 agc ctc ttc tct gat gac cct gaa tct gat cct tct gaa gac aga gcc 4871 Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pro Ser Glu Asp Arg Ala 1570 1575 1580 cca gag tca gct cgt gtt ggc aac ata cca tct tca acc tct gca ttg 4919 Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Ser Ser Thr Ser Ala Leu 1585 1590 1595 1600 aaa gtt ccc caa ttg aaa gtt gca gaa tct gcc cag agt cca gct gct 4967 Lys Val Pro Gln Leu Lys Val Ala Glu Ser Ala Gln Ser Pro Ala Ala 1605 1610 1615 gct cat act act gat act gct ggg tat aat gca atg gaa gaa agt gtg 5015 Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Ala Met Glu Glu Ser Val 1620 1625 1630 agc agg gag aag cca gaa ttg aca gct tca aca gaa agg gtc aac aaa 5063 Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Thr Glu Arg Val Asn Lys 1635 1640 1645 aga atg tcc atg gtg gtg tct ggc ctg acc cca gaa gaa ttt atg ctc 5111 Arg Met Ser Met Val Val Ser Gly Leu Thr Pro Glu Glu Phe Met Leu 1650 1655 1660 gtg tac aag ttt gcc aga aaa cac cac atc act tta act aat cta att 5159 Val Tyr Lys Phe Ala Arg Lys His His Ile Thr Leu Thr Asn Leu Ile 1665 1670 1675 1680 act gaa gag act act cat gtt gtt atg aaa aca gat gct gag ttt gtg 5207 Thr Glu Glu Thr Thr His Val Val Met Lys Thr Asp Ala Glu Phe Val 1685 1690 1695 tgt gaa cgg aca ctg aaa tat ttt cta gga att gcg gga gga aaa tgg 5255 Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Ile Ala Gly Gly Lys Trp 1700 1705 1710 gta gtt agc tat ttc tgg gtg acc cag tct att aaa gaa aga aaa atg 5303 Val Val Ser Tyr Phe Trp Val Thr Gln Ser Ile Lys Glu Arg Lys Met 1715 1720 1725 ctg aat gag cat gat ttt gaa gtc aga gga gat gtg gtc aat gga aga 5351 Leu Asn Glu His Asp Phe Glu Val Arg Gly Asp Val Val Asn Gly Arg 1730 1735 1740 aac cac caa ggt cca aag cga gca aga gaa tcc cag gac aga aag atc 5399 Asn His Gln Gly Pro Lys Arg Ala Arg Glu Ser Gln Asp Arg Lys Ile 1745 1750 1755 1760 ttc agg ggg cta gaa atc tgt tgc tat ggg ccc ttc acc aac atg ccc 5447 Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pro Phe Thr Asn Met Pro 1765 1770 1775 aca gat caa ctg gaa tgg atg gta cag ctg tgt ggt gct tct gtg gtg 5495 Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cys Gly Ala Ser Val Val 1780 1785 1790 aag gag ctt tca tca ttc acc ctt ggc aca ggt gtc cac cca att gtg 5543 Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gly Val His Pro Ile Val 1795 1800 1805 gtt gtg cag cca gat gcc tgg aca gag gac aat ggc ttc cat gca att 5591 ggg cag atg tgt gag gca cct gtg gtg acc cga gag tgg gtg ttg gac 5639 Gly Gln Met Cys Glu Ala Pro Val Val Thr Arg Glu Trp Val Leu Asp 1810 1815 1820 agt gta gca ctc tac cag tgc cag gag ctg gac acc tac ctg ata ccc 5687 Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Leu Ile Pro 1825 1830 1835 1840 cag atc ccc cac agc cac tac tga 5711 Gln Ile Pro His Ser His Tyr 1845 5 21 DNA Artificial Sequence PCR Primer 5 tgctcagggc tatcctctca g 21 6 24 DNA Artificial Sequence PCR Primer 6 tgctggagct ttatcaggtt atgt 24 7 32 DNA Artificial Sequence PCR Probe 7 tgacatttta accactcagc agagggatac ca 32 8 19 DNA Artificial Sequence PCR Primer 8 gaaggtgaag gtcggagtc 19 9 20 DNA Artificial Sequence PCR Primer 9 gaagatggtg atgggatttc 20 10 20 DNA Artificial Sequence PCR Probe 10 caagcttccc gttctcagcc 20 11 7108 DNA H. sapiens CDS (142)...(5733) 11 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca 843 Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr 220 225 230 aat act gaa cat cat caa ccc agt aat aat gat ttg aac acc act gag 891 Asn Thr Glu His His Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu 235 240 245 250 aag cgt gca gct gag agg cat cca gaa aag tat cag ggt agt tct gtt 939 Lys Arg Ala Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Ser Ser Val 255 260 265 tca aac ttg cat gtg gag cca tgt ggc aca aat act cat gcc agc tca 987 Ser Asn Leu His Val Glu Pro Cys Gly Thr Asn Thr His Ala Ser Ser 270 275 280 tta cag cat gag aac agc agt tta tta ctc act aaa gac aga atg aat 1035 Leu Gln His Glu Asn Ser Ser Leu Leu Leu Thr Lys Asp Arg Met Asn 285 290 295 gta gaa aag gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca 1083 Val Glu Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala 300 305 310 agg agc caa cat aac aga tgg gct gga agt aag gaa aca tgt aat gat 1131 Arg Ser Gln His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp 315 320 325 330 agg cgg act ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc 1179 Arg Arg Thr Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro 335 340 345 ctg tgt gag aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag 1227 Leu Cys Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu 350 355 360 aat cct aga gat act gaa gat gtt cct tgg ata aca cta aat agc agc 1275 Asn Pro Arg Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser 365 370 375 att cag aaa gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt 1323 Ile Gln Lys Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly 380 385 390 tct gat gac tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct 1371 Ser Asp Asp Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala 395 400 405 410 gat gta ttg gac gtt cta aat gag gta gat gaa tat tct ggt tct tca 1419 Asp Val Leu Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser 415 420 425 gag aaa ata gac tta ctg gcc agt gat cct cat gag gct tta ata tgt 1467 Glu Lys Ile Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys 430 435 440 aaa agt gaa aga gtt cac tcc aaa tca gta gag agt aat att gaa gac 1515 Lys Ser Glu Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp 445 450 455 aaa ata ttt ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta 1563 Lys Ile Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu 460 465 470 agc cat gta act gaa aat cta att ata gga gca ttt gtt act gag cca 1611 Ser His Val Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro 475 480 485 490 cag ata ata caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg 1659 Gln Ile Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg 495 500 505 aga cct aca tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat 1707 Arg Pro Thr Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp 510 515 520 ttg gca gtt caa aag act cct gaa atg ata aat cag gga act aac caa 1755 Leu Ala Val Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln 525 530 535 acg gag cag aat ggt caa gtg atg aat att act aat agt ggt cat gag 1803 Thr Glu Gln Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu 540 545 550 aat aaa aca aaa ggt gat tct att cag aat gag aaa aat cct aac cca 1851 Asn Lys Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro 555 560 565 570 ata gaa tca ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct 1899 Ile Glu Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro 575 580 585 ata agc agc agt ata agc aat atg gaa ctc gaa tta aat atc cac aat 1947 Ile Ser Ser Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn 590 595 600 tca aaa gca cct aaa aag aat agg ctg agg agg aag tct tct acc agg 1995 Ser Lys Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg 605 610 615 cat att cat gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct 2043 His Ile His Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro 620 625 630 aat tgt act gaa ttg caa att gat agt tgt tct agc agt gaa gag ata 2091 Asn Cys Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile 635 640 645 650 aag aaa aaa aag tac aac caa atg cca gtc agg cac agc aga aac cta 2139 Lys Lys Lys Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu 655 660 665 caa ctc atg gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac 2187 Gln Leu Met Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn 670 675 680 aag cca aat gaa cag aca agt aaa aga cat gac agc gat act ttc cca 2235 Lys Pro Asn Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro 685 690 695 gag ctg aag tta aca aat gca cct ggt tct ttt act aag tgt tca aat 2283 Glu Leu Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn 700 705 710 acc agt gaa ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa 2331 Thr Ser Glu Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu 715 720 725 730 aaa gaa gag aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac 2379 Lys Glu Glu Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp 735 740 745 ccc aaa gat ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga 2427 Pro Lys Asp Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg 750 755 760 tct gta gag agt agc agt att tca ttg gta cct ggt act gat tat ggc 2475 Ser Val Glu Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly 765 770 775 act cag gaa agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca 2523 Thr Gln Glu Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala 780 785 790 aaa aca gaa cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac 2571 Lys Thr Glu Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn 795 800 805 810 ccc aag gga cta att cat ggt tgt tcc aaa gat aat aga aat gac aca 2619 Pro Lys Gly Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr 815 820 825 gaa ggc ttt aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa 2667 Glu Gly Phe Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu 830 835 840 aca agc ata gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag 2715 Thr Ser Ile Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln 845 850 855 aat aca ttc aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat 2763 Asn Thr Phe Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn 860 865 870 cca gga aat gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg 2811 Pro Gly Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly 875 880 885 890 tcc tta aag aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag 2859 Ser Leu Lys Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys 895 900 905 gaa gaa aat caa gga aag aat gag tct aat atc aag cct gta cag aca 2907 Glu Glu Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr 910 915 920 gtt aat atc act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca 2955 Val Asn Ile Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro 925 930 935 gtt gat aat gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta 3003 Val Asp Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu 940 945 950 tca tct cag ttc aga ggc aac gaa act gga ctc att act cca aat aaa 3051 Ser Ser Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys 955 960 965 970 cat gga ctt tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc 3099 His Gly Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile 975 980 985 aag tca ttt gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac 3147 Lys Ser Phe Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn 990 995 1000 ttt gag gaa cat tca atg tca cct gaa aga gaa atg gga aat gag aac 3195 Phe Glu Glu His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn 1005 1010 1015 att cca agt aca gtg agc aca att agc cgt aat aac att aga gaa aat 3243 Ile Pro Ser Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn 1020 1025 1030 gtt ttt aaa gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt 3291 Val Phe Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser 1035 1040 1045 1050 act aat gaa gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa 3339 Thr Asn Glu Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu 1055 1060 1065 aac att caa gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct 3387 Asn Ile Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala 1070 1075 1080 atg ctt aga tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt 3435 Met Leu Arg Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu 1085 1090 1095 cct gga agt aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa 3483 Pro Gly Ser Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu 1100 1105 1110 gaa gta gtt cag act gtt aat aca gat ttc tct cca tat ctg att tca 3531 Glu Val Val Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser 1115 1120 1125 1130 gat aac tta gaa cag cct atg gga agt agt cat gca tct cag gtt tgt 3579 Asp Asn Leu Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys 1135 1140 1145 tct gag aca cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat 3627 Ser Glu Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp 1150 1155 1160 act agt ttt gct gaa aat gac att aag gaa agt tct gct gtt ttt agc 3675 Thr Ser Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser 1165 1170 1175 aaa agc gtc cag aaa gga gag ctt agc agg agt cct agc cct ttc acc 3723 Lys Ser Val Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr 1180 1185 1190 cat aca cat ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag 3771 His Thr His Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu 1195 1200 1205 1210 tcc tca gaa gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc 3819 Ser Ser Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe 1215 1220 1225 caa cac ttg tta ttt ggt aaa gta aac aat ata cct tct cag tct act 3867 Gln His Leu Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr 1230 1235 1240 agg cat agc acc gtt gct acc gag tgt ctg tct aag aac aca gag gag 3915 Arg His Ser Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu 1245 1250 1255 aat tta tta tca ttg aag aat agc tta aat gac tgc agt aac cag gta 3963 Asn Leu Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val 1260 1265 1270 ata ttg gca aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa 4011 Ile Leu Ala Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys 1275 1280 1285 1290 tgt tct gct agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg 4059 Cys Ser Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu 1295 1300 1305 act gca aat aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa 4107 Thr Ala Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys 1310 1315 1320 caa atg agg cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag 4155 Gln Met Arg His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys 1325 1330 1335 gaa ttg gtt tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat 4203 Glu Leu Val Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn 1340 1345 1350 aat caa gaa gag caa agc atg gat tca aac tta ggt gaa gca gca tct 4251 Asn Gln Glu Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser 1355 1360 1365 1370 ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc 4299 Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser 1375 1380 1385 tct cag agt gac att tta acc act cag cag agg gat acc atg caa cat 4347 Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His 1390 1395 1400 aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta 4395 Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu 1405 1410 1415 gaa cag cat ggg agc cag cct tct aac agc tac cct tcc atc ata agt 4443 Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser 1420 1425 1430 gac tct tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca 4491 Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser 1435 1440 1445 1450 gaa aaa gca gta tta act tca cag aaa agt agt gaa tac cct ata agc 4539 Glu Lys Ala Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser 1455 1460 1465 cag aat cca gaa ggc ctt tct gct gac aag ttt gag gtg tct gca gat 4587 Gln Asn Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala Asp 1470 1475 1480 agt tct acc agt aaa aat aaa gaa cca gga gtg gaa agg tca tcc cct 4635 Ser Ser Thr Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Ser Ser Pro 1485 1490 1495 tct aaa tgc cca tca tta gat gat agg tgg tac atg cac agt tgc tct 4683 Ser Lys Cys Pro Ser Leu Asp Asp Arg Trp Tyr Met His Ser Cys Ser 1500 1505 1510 ggg agt ctt cag aat aga aac tac cca tct caa gag gag ctc att aag 4731 Gly Ser Leu Gln Asn Arg Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys 1515 1520 1525 1530 gtt gtt gat gtg gag gag caa cag ctg gaa gag tct ggg cca cac gat 4779 Val Val Asp Val Glu Glu Gln Gln Leu Glu Glu Ser Gly Pro His Asp 1535 1540 1545 ttg acg gaa aca tct tac ttg cca agg caa gat cta gag gga acc cct 4827 Leu Thr Glu Thr Ser Tyr Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro 1550 1555 1560 tac ctg gaa tct gga atc agc ctc ttc tct gat gac cct gaa tct gat 4875 Tyr Leu Glu Ser Gly Ile Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp 1565 1570 1575 cct tct gaa gac aga gcc cca gag tca gct cgt gtt ggc aac ata cca 4923 Pro Ser Glu Asp Arg Ala Pro Glu Ser Ala Arg Val Gly Asn Ile Pro 1580 1585 1590 tct tca acc tct gca ttg aaa gtt ccc caa ttg aaa gtt gca gaa tct 4971 Ser Ser Thr Ser Ala Leu Lys Val Pro Gln Leu Lys Val Ala Glu Ser 1595 1600 1605 1610 gcc cag agt cca gct gct gct cat act act gat act gct ggg tat aat 5019 Ala Gln Ser Pro Ala Ala Ala His Thr Thr Asp Thr Ala Gly Tyr Asn 1615 1620 1625 gca atg gaa gaa agt gtg agc agg gag aag cca gaa ttg aca gct tca 5067 Ala Met Glu Glu Ser Val Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser 1630 1635 1640 aca gaa agg gtc aac aaa aga atg tcc atg gtg gtg tct ggc ctg acc 5115 Thr Glu Arg Val Asn Lys Arg Met Ser Met Val Val Ser Gly Leu Thr 1645 1650 1655 cca gaa gaa ttt atg ctc gtg tac aag ttt gcc aga aaa cac cac atc 5163 Pro Glu Glu Phe Met Leu Val Tyr Lys Phe Ala Arg Lys His His Ile 1660 1665 1670 act tta act aat cta att act gaa gag act act cat gtt gtt atg aaa 5211 Thr Leu Thr Asn Leu Ile Thr Glu Glu Thr Thr His Val Val Met Lys 1675 1680 1685 1690 aca gat gct gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta gga 5259 Thr Asp Ala Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly 1695 1700 1705 att gcg gga gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag tct 5307 Ile Ala Gly Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln Ser 1710 1715 1720 att aaa gaa aga aaa atg ctg aat gag cat gat ttt gaa gtc aga gga 5355 Ile Lys Glu Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg Gly 1725 1730 1735 gat gtg gtc aat gga aga aac cac caa ggt cca aag cga gca aga gaa 5403 Asp Val Val Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg Glu 1740 1745 1750 tcc cag gac aga aag atc ttc agg ggg cta gaa atc tgt tgc tat ggg 5451 Ser Gln Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly 1755 1760 1765 1770 ccc ttc acc aac atg ccc aca gat caa ctg gaa tgg atg gta cag ctg 5499 Pro Phe Thr Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln Leu 1775 1780 1785 tgt ggt gct tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc aca 5547 Cys Gly Ala Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr 1790 1795 1800 ggt gtc cac cca att gtg gtt gtg cag cca gat gcc tgg aca gag gac 5595 Gly Val His Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu Asp 1805 1810 1815 aat ggc ttc cat gca att ggg cag atg tgt gag gca cct gtg gtg acc 5643 Asn Gly Phe His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val Thr 1820 1825 1830 cga gag tgg gtg ttg gac agt gta gca ctc tac cag tgc cag gag ctg 5691 Arg Glu Trp Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu 1835 1840 1845 1850 gac acc tac ctg ata ccc cag atc ccc cac agc cac tac tga ctgcagccag 5743 Asp Thr Tyr Leu Ile Pro Gln Ile Pro His Ser His Tyr 1855 1860 ccacaggtac agagcccagg accccaagaa tgagcttaca aagtggcctt tccaggccct 5803 gggagctcct ctcactcttc agtccttcta ctgtcctggc tactaaatat tttatgtaca 5863 tcagcctgaa aaggacttct ggctatgcaa gggtccctta aagattttct gcttgaagtc 5923 tcccttggaa atctgccatg agcacaaaat tatggtaatt tttcacctga gaagatttta 5983 aaaccattta aacgccacca attgagcaag atgctgattc attatttatc agccctattc 6043 tttctattca ggctgttgtt ggcttagggc tggaagcaca gagtggcttg gcctcaagag 6103 aatagctggt ttccctaagt ttacttctct aaaaccctgt gttcacaaag gcagagagtc 6163 agacccttca atggaaggag agtgcttggg atcgattatg tgacttaaag tcagaatagt 6223 ccttgggcag ttctcaaatg ttggagtgga acattgggga ggaaattctg aggcaggtat 6283 tagaaatgaa aaggaaactt gaaacctggg catggtggct cacgcctgta atcccagcac 6343 tttgggaggc caaggtgggc agatcactgg aggtcaggag ttcgaaacca gcctggccaa 6403 catggtgaaa ccccatctct actaaaaata cagaaattag ccggtcatgg tggtggacac 6463 ctgtaatccc agctactcag gtggctaagg caggagaatc acttcagccc gggaggtgga 6523 ggttgcagtg agccaagatc ataccacggc actccagcct gggtgacagt gagactgtgg 6583 ctcaaaaaaa aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa agtctgagat 6643 atatttgcta gatttctaaa gaatgtgttc taaaacagca gaagattttc aagaaccggt 6703 ttccaaagac agtcttctaa ttcctcatta gtaataagta aaatgtttat tgttgtagct 6763 ctggtatata atccattcct cttaaaatat aagacctctg gcatgaatat ttcatatcta 6823 taaaatgaca gatcccacca ggaaggaagc tgttgctttc tttgaggtga tttttttcct 6883 ttgctccctg ttgctgaaac catacagctt cataaataat tttgcttgct gaaggaagaa 6943 aaagtgtttt tcataaaccc attatccagg actgtttata gctgttggaa ggactaggtc 7003 ttccctagcc cccccagtgt gcaagggcag tgaagacttg attgtacaaa atacgttttg 7063 taaatgttgt gctgttaaca ctgcaaataa acttggtagc aaaca 7108 12 7365 DNA H. sapiens CDS (398)...(5989) 12 ggcagtttgt aggtcgcgag ggaagcgctg aggatcagga agggggcact gagtgtccgt 60 gggggaatcc tcgtgatagg aactggaata tgccttgagg gggacactat gtctttaaaa 120 acgtcggctg gtcatgaggt caggagttcc agaccagcct gaccaacgtg gtgaaactcc 180 gtctctacta aaaatacaaa aattagccgg gcgtggtgcc gctccagcta ctcaggaggc 240 tgaggcagga gaatcgctag aacccgggag gcggaggttg cagtgagccg agatcgcgcc 300 attgcactcc agcctgggcg acagagcgag actgtctcaa aacaaaacaa aacaaaacaa 360 aacaaaaaac accggctgtt cattggaaca gaaagaa atg gat tta tct gct ctt 415 Met Asp Leu Ser Ala Leu 1 5 cgc gtt gaa gaa gta caa aat gtc att aat gct atg cag aaa atc tta 463 Arg Val Glu Glu Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu 10 15 20 gag tgt ccc atc tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag 511 Glu Cys Pro Ile Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys 25 30 35 tgt gac cac ata ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag 559 Cys Asp His Ile Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln 40 45 50 aag aaa ggg cct tca cag tgt cct tta tgt aag aat gat ata acc aaa 607 Lys Lys Gly Pro Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys 55 60 65 70 agg agc cta caa gaa agt acg aga ttt agt caa ctt gtt gaa gag cta 655 Arg Ser Leu Gln Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu 75 80 85 ttg aaa atc att tgt gct ttt cag ctt gac aca ggt ttg gag tat gca 703 Leu Lys Ile Ile Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala 90 95 100 aac agc tat aat ttt gca aaa aag gaa aat aac tct cct gaa cat cta 751 Asn Ser Tyr Asn Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu 105 110 115 aaa gat gaa gtt tct atc atc caa agt atg ggc tac aga aac cgt gcc 799 Lys Asp Glu Val Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala 120 125 130 aaa aga ctt cta cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc 847 Lys Arg Leu Leu Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr 135 140 145 150 agt ctc agt gtc caa ctc tct aac ctt gga act gtg aga act ctg agg 895 Ser Leu Ser Val Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg 155 160 165 aca aag cag cgg ata caa cct caa aag acg tct gtc tac att gaa ttg 943 Thr Lys Gln Arg Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu 170 175 180 gga tct gat tct tct gaa gat acc gtt aat aag gca act tat tgc agt 991 Gly Ser Asp Ser Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser 185 190 195 gtg gga gat caa gaa ttg tta caa atc acc cct caa gga acc agg gat 1039 Val Gly Asp Gln Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp 200 205 210 gaa atc agt ttg gat tct gca aaa aag gct gct tgt gaa ttt tct gag 1087 Glu Ile Ser Leu Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu 215 220 225 230 acg gat gta aca aat act gaa cat cat caa ccc agt aat aat gat ttg 1135 Thr Asp Val Thr Asn Thr Glu His His Gln Pro Ser Asn Asn Asp Leu 235 240 245 aac acc act gag aag cgt gca gct gag agg cat cca gaa aag tat cag 1183 Asn Thr Thr Glu Lys Arg Ala Ala Glu Arg His Pro Glu Lys Tyr Gln 250 255 260 ggt agt tct gtt tca aac ttg cat gtg gag cca tgt ggc aca aat act 1231 Gly Ser Ser Val Ser Asn Leu His Val Glu Pro Cys Gly Thr Asn Thr 265 270 275 cat gcc agc tca tta cag cat gag aac agc agt tta tta ctc act aaa 1279 His Ala Ser Ser Leu Gln His Glu Asn Ser Ser Leu Leu Leu Thr Lys 280 285 290 gac aga atg aat gta gaa aag gct gaa ttc tgt aat aaa agc aaa cag 1327 Asp Arg Met Asn Val Glu Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln 295 300 305 310 cct ggc tta gca agg agc caa cat aac aga tgg gct gga agt aag gaa 1375 Pro Gly Leu Ala Arg Ser Gln His Asn Arg Trp Ala Gly Ser Lys Glu 315 320 325 aca tgt aat gat agg cgg act ccc agc aca gaa aaa aag gta gat ctg 1423 Thr Cys Asn Asp Arg Arg Thr Pro Ser Thr Glu Lys Lys Val Asp Leu 330 335 340 aat gct gat ccc ctg tgt gag aga aaa gaa tgg aat aag cag aaa ctg 1471 Asn Ala Asp Pro Leu Cys Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu 345 350 355 cca tgc tca gag aat cct aga gat act gaa gat gtt cct tgg ata aca 1519 Pro Cys Ser Glu Asn Pro Arg Asp Thr Glu Asp Val Pro Trp Ile Thr 360 365 370 cta aat agc agc att cag aaa gtt aat gag tgg ttt tcc aga agt gat 1567 Leu Asn Ser Ser Ile Gln Lys Val Asn Glu Trp Phe Ser Arg Ser Asp 375 380 385 390 gaa ctg tta ggt tct gat gac tca cat gat ggg gag tct gaa tca aat 1615 Glu Leu Leu Gly Ser Asp Asp Ser His Asp Gly Glu Ser Glu Ser Asn 395 400 405 gcc aaa gta gct gat gta ttg gac gtt cta aat gag gta gat gaa tat 1663 Ala Lys Val Ala Asp Val Leu Asp Val Leu Asn Glu Val Asp Glu Tyr 410 415 420 tct ggt tct tca gag aaa ata gac tta ctg gcc agt gat cct cat gag 1711 Ser Gly Ser Ser Glu Lys Ile Asp Leu Leu Ala Ser Asp Pro His Glu 425 430 435 gct tta ata tgt aaa agt gaa aga gtt cac tcc aaa tca gta gag agt 1759 Ala Leu Ile Cys Lys Ser Glu Arg Val His Ser Lys Ser Val Glu Ser 440 445 450 aat att gaa gac aaa ata ttt ggg aaa acc tat cgg aag aag gca agc 1807 Asn Ile Glu Asp Lys Ile Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser 455 460 465 470 ctc ccc aac tta agc cat gta act gaa aat cta att ata gga gca ttt 1855 Leu Pro Asn Leu Ser His Val Thr Glu Asn Leu Ile Ile Gly Ala Phe 475 480 485 gtt act gag cca cag ata ata caa gag cgt ccc ctc aca aat aaa tta 1903 Val Thr Glu Pro Gln Ile Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu 490 495 500 aag cgt aaa agg aga cct aca tca ggc ctt cat cct gag gat ttt atc 1951 Lys Arg Lys Arg Arg Pro Thr Ser Gly Leu His Pro Glu Asp Phe Ile 505 510 515 aag aaa gca gat ttg gca gtt caa aag act cct gaa atg ata aat cag 1999 Lys Lys Ala Asp Leu Ala Val Gln Lys Thr Pro Glu Met Ile Asn Gln 520 525 530 gga act aac caa acg gag cag aat ggt caa gtg atg aat att act aat 2047 Gly Thr Asn Gln Thr Glu Gln Asn Gly Gln Val Met Asn Ile Thr Asn 535 540 545 550 agt ggt cat gag aat aaa aca aaa ggt gat tct att cag aat gag aaa 2095 Ser Gly His Glu Asn Lys Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys 555 560 565 aat cct aac cca ata gaa tca ctc gaa aaa gaa tct gct ttc aaa acg 2143 Asn Pro Asn Pro Ile Glu Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr 570 575 580 aaa gct gaa cct ata agc agc agt ata agc aat atg gaa ctc gaa tta 2191 Lys Ala Glu Pro Ile Ser Ser Ser Ile Ser Asn Met Glu Leu Glu Leu 585 590 595 aat atc cac aat tca aaa gca cct aaa aag aat agg ctg agg agg aag 2239 Asn Ile His Asn Ser Lys Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys 600 605 610 tct tct acc agg cat att cat gcg ctt gaa cta gta gtc agt aga aat 2287 Ser Ser Thr Arg His Ile His Ala Leu Glu Leu Val Val Ser Arg Asn 615 620 625 630 cta agc cca cct aat tgt act gaa ttg caa att gat agt tgt tct agc 2335 Leu Ser Pro Pro Asn Cys Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser 635 640 645 agt gaa gag ata aag aaa aaa aag tac aac caa atg cca gtc agg cac 2383 Ser Glu Glu Ile Lys Lys Lys Lys Tyr Asn Gln Met Pro Val Arg His 650 655 660 agc aga aac cta caa ctc atg gaa ggt aaa gaa cct gca act gga gcc 2431 Ser Arg Asn Leu Gln Leu Met Glu Gly Lys Glu Pro Ala Thr Gly Ala 665 670 675 aag aag agt aac aag cca aat gaa cag aca agt aaa aga cat gac agc 2479 Lys Lys Ser Asn Lys Pro Asn Glu Gln Thr Ser Lys Arg His Asp Ser 680 685 690 gat act ttc cca gag ctg aag tta aca aat gca cct ggt tct ttt act 2527 Asp Thr Phe Pro Glu Leu Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr 695 700 705 710 aag tgt tca aat acc agt gaa ctt aaa gaa ttt gtc aat cct agc ctt 2575 Lys Cys Ser Asn Thr Ser Glu Leu Lys Glu Phe Val Asn Pro Ser Leu 715 720 725 cca aga gaa gaa aaa gaa gag aaa cta gaa aca gtt aaa gtg tct aat 2623 Pro Arg Glu Glu Lys Glu Glu Lys Leu Glu Thr Val Lys Val Ser Asn 730 735 740 aat gct gaa gac ccc aaa gat ctc atg tta agt gga gaa agg gtt ttg 2671 Asn Ala Glu Asp Pro Lys Asp Leu Met Leu Ser Gly Glu Arg Val Leu 745 750 755 caa act gaa aga tct gta gag agt agc agt att tca ttg gta cct ggt 2719 Gln Thr Glu Arg Ser Val Glu Ser Ser Ser Ile Ser Leu Val Pro Gly 760 765 770 act gat tat ggc act cag gaa agt atc tcg tta ctg gaa gtt agc act 2767 Thr Asp Tyr Gly Thr Gln Glu Ser Ile Ser Leu Leu Glu Val Ser Thr 775 780 785 790 cta ggg aag gca aaa aca gaa cca aat aaa tgt gtg agt cag tgt gca 2815 Leu Gly Lys Ala Lys Thr Glu Pro Asn Lys Cys Val Ser Gln Cys Ala 795 800 805 gca ttt gaa aac ccc aag gga cta att cat ggt tgt tcc aaa gat aat 2863 Ala Phe Glu Asn Pro Lys Gly Leu Ile His Gly Cys Ser Lys Asp Asn 810 815 820 aga aat gac aca gaa ggc ttt aag tat cca ttg gga cat gaa gtt aac 2911 Arg Asn Asp Thr Glu Gly Phe Lys Tyr Pro Leu Gly His Glu Val Asn 825 830 835 cac agt cgg gaa aca agc ata gaa atg gaa gaa agt gaa ctt gat gct 2959 His Ser Arg Glu Thr Ser Ile Glu Met Glu Glu Ser Glu Leu Asp Ala 840 845 850 cag tat ttg cag aat aca ttc aag gtt tca aag cgc cag tca ttt gct 3007 Gln Tyr Leu Gln Asn Thr Phe Lys Val Ser Lys Arg Gln Ser Phe Ala 855 860 865 870 ccg ttt tca aat cca gga aat gca gaa gag gaa tgt gca aca ttc tct 3055 Pro Phe Ser Asn Pro Gly Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser 875 880 885 gcc cac tct ggg tcc tta aag aaa caa agt cca aaa gtc act ttt gaa 3103 Ala His Ser Gly Ser Leu Lys Lys Gln Ser Pro Lys Val Thr Phe Glu 890 895 900 tgt gaa caa aag gaa gaa aat caa gga aag aat gag tct aat atc aag 3151 Cys Glu Gln Lys Glu Glu Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys 905 910 915 cct gta cag aca gtt aat atc act gca ggc ttt cct gtg gtt ggt cag 3199 Pro Val Gln Thr Val Asn Ile Thr Ala Gly Phe Pro Val Val Gly Gln 920 925 930 aaa gat aag cca gtt gat aat gcc aaa tgt agt atc aaa gga ggc tct 3247 Lys Asp Lys Pro Val Asp Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser 935 940 945 950 agg ttt tgt cta tca tct cag ttc aga ggc aac gaa act gga ctc att 3295 Arg Phe Cys Leu Ser Ser Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile 955 960 965 act cca aat aaa cat gga ctt tta caa aac cca tat cgt ata cca cca 3343 Thr Pro Asn Lys His Gly Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro 970 975 980 ctt ttt ccc atc aag tca ttt gtt aaa act aaa tgt aag aaa aat ctg 3391 Leu Phe Pro Ile Lys Ser Phe Val Lys Thr Lys Cys Lys Lys Asn Leu 985 990 995 cta gag gaa aac ttt gag gaa cat tca atg tca cct gaa aga gaa atg 3439 Leu Glu Glu Asn Phe Glu Glu His Ser Met Ser Pro Glu Arg Glu Met 1000 1005 1010 gga aat gag aac att cca agt aca gtg agc aca att agc cgt aat aac 3487 Gly Asn Glu Asn Ile Pro Ser Thr Val Ser Thr Ile Ser Arg Asn Asn 1015 1020 1025 1030 att aga gaa aat gtt ttt aaa gaa gcc agc tca agc aat att aat gaa 3535 Ile Arg Glu Asn Val Phe Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu 1035 1040 1045 gta ggt tcc agt act aat gaa gtg ggc tcc agt att aat gaa ata ggt 3583 Val Gly Ser Ser Thr Asn Glu Val Gly Ser Ser Ile Asn Glu Ile Gly 1050 1055 1060 tcc agt gat gaa aac att caa gca gaa cta ggt aga aac aga ggg cca 3631 Ser Ser Asp Glu Asn Ile Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro 1065 1070 1075 aaa ttg aat gct atg ctt aga tta ggg gtt ttg caa cct gag gtc tat 3679 Lys Leu Asn Ala Met Leu Arg Leu Gly Val Leu Gln Pro Glu Val Tyr 1080 1085 1090 aaa caa agt ctt cct gga agt aat tgt aag cat cct gaa ata aaa aag 3727 Lys Gln Ser Leu Pro Gly Ser Asn Cys Lys His Pro Glu Ile Lys Lys 1095 1100 1105 1110 caa gaa tat gaa gaa gta gtt cag act gtt aat aca gat ttc tct cca 3775 Gln Glu Tyr Glu Glu Val Val Gln Thr Val Asn Thr Asp Phe Ser Pro 1115 1120 1125 tat ctg att tca gat aac tta gaa cag cct atg gga agt agt cat gca 3823 Tyr Leu Ile Ser Asp Asn Leu Glu Gln Pro Met Gly Ser Ser His Ala 1130 1135 1140 tct cag gtt tgt tct gag aca cct gat gac ctg tta gat gat ggt gaa 3871 Ser Gln Val Cys Ser Glu Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu 1145 1150 1155 ata aag gaa gat act agt ttt gct gaa aat gac att aag gaa agt tct 3919 Ile Lys Glu Asp Thr Ser Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser 1160 1165 1170 gct gtt ttt agc aaa agc gtc cag aaa gga gag ctt agc agg agt cct 3967 Ala Val Phe Ser Lys Ser Val Gln Lys Gly Glu Leu Ser Arg Ser Pro 1175 1180 1185 1190 agc cct ttc acc cat aca cat ttg gct cag ggt tac cga aga ggg gcc 4015 Ser Pro Phe Thr His Thr His Leu Ala Gln Gly Tyr Arg Arg Gly Ala 1195 1200 1205 aag aaa tta gag tcc tca gaa gag aac tta tct agt gag gat gaa gag 4063 Lys Lys Leu Glu Ser Ser Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu 1210 1215 1220 ctt ccc tgc ttc caa cac ttg tta ttt ggt aaa gta aac aat ata cct 4111 Leu Pro Cys Phe Gln His Leu Leu Phe Gly Lys Val Asn Asn Ile Pro 1225 1230 1235 tct cag tct act agg cat agc acc gtt gct acc gag tgt ctg tct aag 4159 Ser Gln Ser Thr Arg His Ser Thr Val Ala Thr Glu Cys Leu Ser Lys 1240 1245 1250 aac aca gag gag aat tta tta tca ttg aag aat agc tta aat gac tgc 4207 Asn Thr Glu Glu Asn Leu Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys 1255 1260 1265 1270 agt aac cag gta ata ttg gca aag gca tct cag gaa cat cac ctt agt 4255 Ser Asn Gln Val Ile Leu Ala Lys Ala Ser Gln Glu His His Leu Ser 1275 1280 1285 gag gaa aca aaa tgt tct gct agc ttg ttt tct tca cag tgc agt gaa 4303 Glu Glu Thr Lys Cys Ser Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu 1290 1295 1300 ttg gaa gac ttg act gca aat aca aac acc cag gat cct ttc ttg att 4351 Leu Glu Asp Leu Thr Ala Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile 1305 1310 1315 ggt tct tcc aaa caa atg agg cat cag tct gaa agc cag gga gtt ggt 4399 Gly Ser Ser Lys Gln Met Arg His Gln Ser Glu Ser Gln Gly Val Gly 1320 1325 1330 ctg agt gac aag gaa ttg gtt tca gat gat gaa gaa aga gga acg ggc 4447 Leu Ser Asp Lys Glu Leu Val Ser Asp Asp Glu Glu Arg Gly Thr Gly 1335 1340 1345 1350 ttg gaa gaa aat aat caa gaa gag caa agc atg gat tca aac tta ggt 4495 Leu Glu Glu Asn Asn Gln Glu Glu Gln Ser Met Asp Ser Asn Leu Gly 1355 1360 1365 gaa gca gca tct ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc 4543 Glu Ala Ala Ser Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys 1370 1375 1380 tca ggg cta tcc tct cag agt gac att tta acc act cag cag agg gat 4591 Ser Gly Leu Ser Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp 1385 1390 1395 acc atg caa cat aac ctg ata aag ctc cag cag gaa atg gct gaa cta 4639 Thr Met Gln His Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu 1400 1405 1410 gaa gct gtg tta gaa cag cat ggg agc cag cct tct aac agc tac cct 4687 Glu Ala Val Leu Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro 1415 1420 1425 1430 tcc atc ata agt gac tct tct gcc ctt gag gac ctg cga aat cca gaa 4735 Ser Ile Ile Ser Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu 1435 1440 1445 caa agc aca tca gaa aaa gca gta tta act tca cag aaa agt agt gaa 4783 Gln Ser Thr Ser Glu Lys Ala Val Leu Thr Ser Gln Lys Ser Ser Glu 1450 1455 1460 tac cct ata agc cag aat cca gaa ggc ctt tct gct gac aag ttt gag 4831 Tyr Pro Ile Ser Gln Asn Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu 1465 1470 1475 gtg tct gca gat agt tct acc agt aaa aat aaa gaa cca gga gtg gaa 4879 Val Ser Ala Asp Ser Ser Thr Ser Lys Asn Lys Glu Pro Gly Val Glu 1480 1485 1490 agg tca tcc cct tct aaa tgc cca tca tta gat gat agg tgg tac atg 4927 Arg Ser Ser Pro Ser Lys Cys Pro Ser Leu Asp Asp Arg Trp Tyr Met 1495 1500 1505 1510 cac agt tgc tct ggg agt ctt cag aat aga aac tac cca tct caa gag 4975 His Ser Cys Ser Gly Ser Leu Gln Asn Arg Asn Tyr Pro Ser Gln Glu 1515 1520 1525 gag ctc att aag gtt gtt gat gtg gag gag caa cag ctg gaa gag tct 5023 Glu Leu Ile Lys Val Val Asp Val Glu Glu Gln Gln Leu Glu Glu Ser 1530 1535 1540 ggg cca cac gat ttg acg gaa aca tct tac ttg cca agg caa gat cta 5071 Gly Pro His Asp Leu Thr Glu Thr Ser Tyr Leu Pro Arg Gln Asp Leu 1545 1550 1555 gag gga acc cct tac ctg gaa tct gga atc agc ctc ttc tct gat gac 5119 Glu Gly Thr Pro Tyr Leu Glu Ser Gly Ile Ser Leu Phe Ser Asp Asp 1560 1565 1570 cct gaa tct gat cct tct gaa gac aga gcc cca gag tca gct cgt gtt 5167 Pro Glu Ser Asp Pro Ser Glu Asp Arg Ala Pro Glu Ser Ala Arg Val 1575 1580 1585 1590 ggc aac ata cca tct tca acc tct gca ttg aaa gtt ccc caa ttg aaa 5215 Gly Asn Ile Pro Ser Ser Thr Ser Ala Leu Lys Val Pro Gln Leu Lys 1595 1600 1605 gtt gca gaa tct gcc cag agt cca gct gct gct cat act act gat act 5263 Val Ala Glu Ser Ala Gln Ser Pro Ala Ala Ala His Thr Thr Asp Thr 1610 1615 1620 gct ggg tat aat gca atg gaa gaa agt gtg agc agg gag aag cca gaa 5311 Ala Gly Tyr Asn Ala Met Glu Glu Ser Val Ser Arg Glu Lys Pro Glu 1625 1630 1635 ttg aca gct tca aca gaa agg gtc aac aaa aga atg tcc atg gtg gtg 5359 Leu Thr Ala Ser Thr Glu Arg Val Asn Lys Arg Met Ser Met Val Val 1640 1645 1650 tct ggc ctg acc cca gaa gaa ttt atg ctc gtg tac aag ttt gcc aga 5407 Ser Gly Leu Thr Pro Glu Glu Phe Met Leu Val Tyr Lys Phe Ala Arg 1655 1660 1665 1670 aaa cac cac atc act tta act aat cta att act gaa gag act act cat 5455 Lys His His Ile Thr Leu Thr Asn Leu Ile Thr Glu Glu Thr Thr His 1675 1680 1685 gtt gtt atg aaa aca gat gct gag ttt gtg tgt gaa cgg aca ctg aaa 5503 Val Val Met Lys Thr Asp Ala Glu Phe Val Cys Glu Arg Thr Leu Lys 1690 1695 1700 tat ttt cta gga att gcg gga gga aaa tgg gta gtt agc tat ttc tgg 5551 Tyr Phe Leu Gly Ile Ala Gly Gly Lys Trp Val Val Ser Tyr Phe Trp 1705 1710 1715 gtg acc cag tct att aaa gaa aga aaa atg ctg aat gag cat gat ttt 5599 Val Thr Gln Ser Ile Lys Glu Arg Lys Met Leu Asn Glu His Asp Phe 1720 1725 1730 gaa gtc aga gga gat gtg gtc aat gga aga aac cac caa ggt cca aag 5647 Glu Val Arg Gly Asp Val Val Asn Gly Arg Asn His Gln Gly Pro Lys 1735 1740 1745 1750 cga gca aga gaa tcc cag gac aga aag atc ttc agg ggg cta gaa atc 5695 Arg Ala Arg Glu Ser Gln Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile 1755 1760 1765 tgt tgc tat ggg ccc ttc acc aac atg ccc aca gat caa ctg gaa tgg 5743 Cys Cys Tyr Gly Pro Phe Thr Asn Met Pro Thr Asp Gln Leu Glu Trp 1770 1775 1780 atg gta cag ctg tgt ggt gct tct gtg gtg aag gag ctt tca tca ttc 5791 Met Val Gln Leu Cys Gly Ala Ser Val Val Lys Glu Leu Ser Ser Phe 1785 1790 1795 acc ctt ggc aca ggt gtc cac cca att gtg gtt gtg cag cca gat gcc 5839 Thr Leu Gly Thr Gly Val His Pro Ile Val Val Val Gln Pro Asp Ala 1800 1805 1810 tgg aca gag gac aat ggc ttc cat gca att ggg cag atg tgt gag gca 5887 Trp Thr Glu Asp Asn Gly Phe His Ala Ile Gly Gln Met Cys Glu Ala 1815 1820 1825 1830 cct gtg gtg acc cga gag tgg gtg ttg gac agt gta gca ctc tac cag 5935 Pro Val Val Thr Arg Glu Trp Val Leu Asp Ser Val Ala Leu Tyr Gln 1835 1840 1845 tgc cag gag ctg gac acc tac ctg ata ccc cag atc ccc cac agc cac 5983 Cys Gln Glu Leu Asp Thr Tyr Leu Ile Pro Gln Ile Pro His Ser His 1850 1855 1860 tac tga ctgcagccag ccacaggtac agagccacag gaccccaaga atgagcttac 6039 Tyr aaagtggcct ttccaggccc tgggagctcc tctcactctt cagtccttct actgtcctgg 6099 ctactaaata ttttatgtac atcagcctga aaaggacttc tggctatgca agggtccctt 6159 aaagattttc tgcttgaagt ctcccttgga aatctgccat gagcacaaaa ttatggtaat 6219 ttttcacctg agaagatttt aaaaccattt aaacgccacc aattgagcaa gatgctgatt 6279 cattatttat cagccctatt ctttctattc aggctgttgt tggcttaggg ctggaagcac 6339 agagtggctt ggcctcaaga gaatagctgg tttccctaag tttacttctc taaaaccctg 6399 tgttcacaaa ggcagagagt cagacccttc aatggaagga gagtgcttgg gatcgattat 6459 gtgacttaaa gtcagaatag tccttgggca gttctcaaat gttggagtgg aacattgggg 6519 aggaaattct gaggcaggta ttagaaatga aaaggaaact tgaaacctgg gcatggtggc 6579 tcacgcctgt aatcccagca ctttgggagg ccaaggtggg cagatcactg gaggtcagga 6639 gttcgaaacc agcctggcca acatggtgaa accccatctc tactaaaaat acagaaatta 6699 gccggtcatg gtggtggaca cctgtaatcc cagctactca ggtggctaag gcaggagaat 6759 cacttcagcc cgggaggtgg aggttgcagt gagccaagat cataccacgg cactccagcc 6819 tgggtgacag tgagactgtg gctcaaaaaa aaaaaaaaaa aaggaaaatg aaactaggaa 6879 aggtttctta aagtctgaga tatatttgct agatttctaa agaatgtgtt ctaaaacagc 6939 agaagatttt caagaaccgg tttccaaaga cagtcttcta attcctcatt agtaataagt 6999 aaaatgttta ttgttgtagc tctggtatat aatccattcc tcttaaaata taagacctct 7059 ggcatgaata tttcatatct ataaaatgac agatcccacc aggaaggaag ctgttgcttt 7119 ctttgaggtg atttttttcc tttgctccct gttgctgaaa ccatacagct tcataaataa 7179 ttttgcttgc tgaaggaaga aaaagtgttt ttcataaacc cattatccag gactgtttat 7239 agctgttgga aggactaggt cttccctagc ccccccagtg tgcaagggca gtgaagactt 7299 gattgtacaa aatacgtttt gtaaatgttg tgctgttaac actgcaaata aacttggtag 7359 caaaca 7365 13 7102 DNA H. sapiens CDS (136)...(5727) 13 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctggttca 120 ttggaacaga aagaa atg gat tta tct gct ctt cgc gtt gaa gaa gta caa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu Val Gln 1 5 10 aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc tgt ctg 219 Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile Cys Leu 15 20 25 gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata ttt tgc 267 Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile Phe Cys 30 35 40 aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct tca cag 315 Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro Ser Gln 45 50 55 60 tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa gaa agt 363 Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln Glu Ser 65 70 75 acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att tgt gct 411 Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile Cys Ala 80 85 90 ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat ttt gca 459 Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn Phe Ala 95 100 105 aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt tct atc 507 Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val Ser Ile 110 115 120 atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta cag agt 555 Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu Gln Ser 125 130 135 140 gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc caa ctc 603 Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val Gln Leu 145 150 155 tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg ata caa 651 Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg Ile Gln 160 165 170 cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct tct gaa 699 Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser Ser Glu 175 180 185 gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa gaa ttg 747 Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln Glu Leu 190 195 200 tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg gat tct 795 Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu Asp Ser 205 210 215 220 gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca aat act 843 Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr Asn Thr 225 230 235 gaa cat cat caa ccc agt aat aat gat ttg aac acc act gag aag cgt 891 Glu His His Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu Lys Arg 240 245 250 gca gct gag agg cat cca gaa aag tat cag ggt agt tct gtt tca aac 939 Ala Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Ser Ser Val Ser Asn 255 260 265 ttg cat gtg gag cca tgt ggc aca aat act cat gcc agc tca tta cag 987 Leu His Val Glu Pro Cys Gly Thr Asn Thr His Ala Ser Ser Leu Gln 270 275 280 cat gag aac agc agt tta tta ctc act aaa gac aga atg aat gta gaa 1035 His Glu Asn Ser Ser Leu Leu Leu Thr Lys Asp Arg Met Asn Val Glu 285 290 295 300 aag gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca agg agc 1083 Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala Arg Ser 305 310 315 caa cat aac aga tgg gct gga agt aag gaa aca tgt aat gat agg cgg 1131 Gln His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp Arg Arg 320 325 330 act ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc ctg tgt 1179 Thr Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro Leu Cys 335 340 345 gag aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag aat cct 1227 Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu Asn Pro 350 355 360 aga gat act gaa gat gtt cct tgg ata aca cta aat agc agc att cag 1275 Arg Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser Ile Gln 365 370 375 380 aaa gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt tct gat 1323 Lys Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly Ser Asp 385 390 395 gac tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct gat gta 1371 Asp Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala Asp Val 400 405 410 ttg gac gtt cta aat gag gta gat gaa tat tct ggt tct tca gag aaa 1419 Leu Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser Glu Lys 415 420 425 ata gac tta ctg gcc agt gat cct cat gag gct tta ata tgt aaa agt 1467 Ile Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys Lys Ser 430 435 440 gaa aga gtt cac tcc aaa tca gta gag agt aat att gaa gac aaa ata 1515 Glu Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp Lys Ile 445 450 455 460 ttt ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta agc cat 1563 Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu Ser His 465 470 475 gta act gaa aat cta att ata gga gca ttt gtt act gag cca cag ata 1611 Val Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro Gln Ile 480 485 490 ata caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg aga cct 1659 Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg Arg Pro 495 500 505 aca tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat ttg gca 1707 Thr Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp Leu Ala 510 515 520 gtt caa aag act cct gaa atg ata aat cag gga act aac caa acg gag 1755 Val Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln Thr Glu 525 530 535 540 cag aat ggt caa gtg atg aat att act aat agt ggt cat gag aat aaa 1803 Gln Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu Asn Lys 545 550 555 aca aaa ggt gat tct att cag aat gag aaa aat cct aac cca ata gaa 1851 Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro Ile Glu 560 565 570 tca ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct ata agc 1899 Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro Ile Ser 575 580 585 agc agt ata agc aat atg gaa ctc gaa tta aat atc cac aat tca aaa 1947 Ser Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn Ser Lys 590 595 600 gca cct aaa aag aat agg ctg agg agg aag tct tct acc agg cat att 1995 Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg His Ile 605 610 615 620 cat gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct aat tgt 2043 His Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro Asn Cys 625 630 635 act gaa ttg caa att gat agt tgt tct agc agt gaa gag ata aag aaa 2091 Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile Lys Lys 640 645 650 aaa aag tac aac caa atg cca gtc agg cac agc aga aac cta caa ctc 2139 Lys Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu Gln Leu 655 660 665 atg gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac aag cca 2187 Met Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn Lys Pro 670 675 680 aat gaa cag aca agt aaa aga cat gac agc gat act ttc cca gag ctg 2235 Asn Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro Glu Leu 685 690 695 700 aag tta aca aat gca cct ggt tct ttt act aag tgt tca aat acc agt 2283 Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn Thr Ser 705 710 715 gaa ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa aaa gaa 2331 Glu Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu Lys Glu 720 725 730 gag aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac ccc aaa 2379 Glu Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp Pro Lys 735 740 745 gat ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga tct gta 2427 Asp Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg Ser Val 750 755 760 gag agt agc agt att tca ttg gta cct ggt act gat tat ggc act cag 2475 Glu Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly Thr Gln 765 770 775 780 gaa agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca aaa aca 2523 Glu Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala Lys Thr 785 790 795 gaa cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac ccc aag 2571 Glu Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn Pro Lys 800 805 810 gga cta att cat ggt tgt tcc aaa gat aat aga aat gac aca gaa ggc 2619 Gly Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr Glu Gly 815 820 825 ttt aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa aca agc 2667 Phe Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu Thr Ser 830 835 840 ata gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag aat aca 2715 Ile Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln Asn Thr 845 850 855 860 ttc aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat cca gga 2763 Phe Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn Pro Gly 865 870 875 aat gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg tcc tta 2811 Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly Ser Leu 880 885 890 aag aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag gaa gaa 2859 Lys Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys Glu Glu 895 900 905 aat caa gga aag aat gag tct aat atc aag cct gta cag aca gtt aat 2907 Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr Val Asn 910 915 920 atc act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca gtt gat 2955 Ile Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro Val Asp 925 930 935 940 aat gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta tca tct 3003 Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu Ser Ser 945 950 955 cag ttc aga ggc aac gaa act gga ctc att act cca aat aaa cat gga 3051 Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys His Gly 960 965 970 ctt tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc aag tca 3099 Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile Lys Ser 975 980 985 ttt gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac ttt gag 3147 Phe Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn Phe Glu 990 995 1000 gaa cat tca atg tca cct gaa aga gaa atg gga aat gag aac att cca 3195 Glu His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn Ile Pro 1005 1010 1015 1020 agt aca gtg agc aca att agc cgt aat aac att aga gaa aat gtt ttt 3243 Ser Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn Val Phe 1025 1030 1035 aaa gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt act aat 3291 Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser Thr Asn 1040 1045 1050 gaa gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa aac att 3339 Glu Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu Asn Ile 1055 1060 1065 caa gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct atg ctt 3387 Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala Met Leu 1070 1075 1080 aga tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt cct gga 3435 Arg Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu Pro Gly 1085 1090 1095 1100 agt aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa gaa gta 3483 Ser Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu Glu Val 1105 1110 1115 gtt cag act gtt aat aca gat ttc tct cca tat ctg att tca gat aac 3531 Val Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser Asp Asn 1120 1125 1130 tta gaa cag cct atg gga agt agt cat gca tct cag gtt tgt tct gag 3579 Leu Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys Ser Glu 1135 1140 1145 aca cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat act agt 3627 Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp Thr Ser 1150 1155 1160 ttt gct gaa aat gac att aag gaa agt tct gct gtt ttt agc aaa agc 3675 Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser Lys Ser 1165 1170 1175 1180 gtc cag aaa gga gag ctt agc agg agt cct agc cct ttc acc cat aca 3723 Val Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr His Thr 1185 1190 1195 cat ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag tcc tca 3771 His Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu Ser Ser 1200 1205 1210 gaa gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc caa cac 3819 Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe Gln His 1215 1220 1225 ttg tta ttt ggt aaa gta aac aat ata cct tct cag tct act agg cat 3867 Leu Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr Arg His 1230 1235 1240 agc acc gtt gct acc gag tgt ctg tct aag aac aca gag gag aat tta 3915 Ser Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu Asn Leu 1245 1250 1255 1260 tta tca ttg aag aat agc tta aat gac tgc agt aac cag gta ata ttg 3963 Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val Ile Leu 1265 1270 1275 gca aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa tgt tct 4011 Ala Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys Cys Ser 1280 1285 1290 gct agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg act gca 4059 Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu Thr Ala 1295 1300 1305 aat aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa caa atg 4107 Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys Gln Met 1310 1315 1320 agg cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag gaa ttg 4155 Arg His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys Glu Leu 1325 1330 1335 1340 gtt tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat aat caa 4203 Val Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn Asn Gln 1345 1350 1355 gaa gag caa agc atg gat tca aac tta ggt gaa gca gca tct ggg tgt 4251 Glu Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser Gly Cys 1360 1365 1370 gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc tct cag 4299 Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Ser Gln 1375 1380 1385 agt gac att tta acc act cag cag agg gat acc atg caa cat aac ctg 4347 Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His Asn Leu 1390 1395 1400 ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta gaa cag 4395 Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu Glu Gln 1405 1410 1415 1420 cat ggg agc cag cct tct aac agc tac cct tcc atc ata agt gac tct 4443 His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser Asp Ser 1425 1430 1435 tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca gaa aaa 4491 Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Glu Lys 1440 1445 1450 gca gta tta act tca cag aaa agt agt gaa tac cct ata agc cag aat 4539 Ala Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gln Asn 1455 1460 1465 cca gaa ggc ctt tct gct gac aag ttt gag gtg tct gca gat agt tct 4587 Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Ser Ser 1470 1475 1480 acc agt aaa aat aaa gaa cca gga gtg gaa agg tca tcc cct tct aaa 4635 Thr Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Ser Lys 1485 1490 1495 1500 tgc cca tca tta gat gat agg tgg tac atg cac agt tgc tct ggg agt 4683 Cys Pro Ser Leu Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gly Ser 1505 1510 1515 ctt cag aat aga aac tac cca tct caa gag gag ctc att aag gtt gtt 4731 Leu Gln Asn Arg Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys Val Val 1520 1525 1530 gat gtg gag gag caa cag ctg gaa gag tct ggg cca cac gat ttg acg 4779 Asp Val Glu Glu Gln Gln Leu Glu Glu Ser Gly Pro His Asp Leu Thr 1535 1540 1545 gaa aca tct tac ttg cca agg caa gat cta gag gga acc cct tac ctg 4827 Glu Thr Ser Tyr Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Tyr Leu 1550 1555 1560 gaa tct gga atc agc ctc ttc tct gat gac cct gaa tct gat cct tct 4875 Glu Ser Gly Ile Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pro Ser 1565 1570 1575 1580 gaa gac aga gcc cca gag tca gct cgt gtt ggc aac ata cca tct tca 4923 Glu Asp Arg Ala Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Ser Ser 1585 1590 1595 acc tct gca ttg aaa gtt ccc caa ttg aaa gtt gca gaa tct gcc cag 4971 Thr Ser Ala Leu Lys Val Pro Gln Leu Lys Val Ala Glu Ser Ala Gln 1600 1605 1610 agt cca gct gct gct cat act act gat act gct ggg tat aat gca atg 5019 Ser Pro Ala Ala Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Ala Met 1615 1620 1625 gaa gaa agt gtg agc agg gag aag cca gaa ttg aca gct tca aca gaa 5067 Glu Glu Ser Val Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Thr Glu 1630 1635 1640 agg gtc aac aaa aga atg tcc atg gtg gtg tct ggc ctg acc cca gaa 5115 Arg Val Asn Lys Arg Met Ser Met Val Val Ser Gly Leu Thr Pro Glu 1645 1650 1655 1660 gaa ttt atg ctc gtg tac aag ttt gcc aga aaa cac cac atc act tta 5163 Glu Phe Met Leu Val Tyr Lys Phe Ala Arg Lys His His Ile Thr Leu 1665 1670 1675 act aat cta att act gaa gag act act cat gtt gtt atg aaa aca gat 5211 Thr Asn Leu Ile Thr Glu Glu Thr Thr His Val Val Met Lys Thr Asp 1680 1685 1690 gct gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta gga att gcg 5259 Ala Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Ile Ala 1695 1700 1705 gga gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag tct att aaa 5307 Gly Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln Ser Ile Lys 1710 1715 1720 gaa aga aaa atg ctg aat gag cat gat ttt gaa gtc aga gga gat gtg 5355 Glu Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg Gly Asp Val 1725 1730 1735 1740 gtc aat gga aga aac cac caa ggt cca aag cga gca aga gaa tcc cag 5403 Val Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg Glu Ser Gln 1745 1750 1755 gac aga aag atc ttc agg ggg cta gaa atc tgt tgc tat ggg ccc ttc 5451 Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pro Phe 1760 1765 1770 acc aac atg ccc aca gat caa ctg gaa tgg atg gta cag ctg tgt ggt 5499 Thr Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cys Gly 1775 1780 1785 gct tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc aca ggt gtc 5547 Ala Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gly Val 1790 1795 1800 cac cca att gtg gtt gtg cag cca gat gcc tgg aca gag gac aat ggc 5595 His Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu Asp Asn Gly 1805 1810 1815 1820 ttc cat gca att ggg cag atg tgt gag gca cct gtg gtg acc cga gag 5643 Phe His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val Thr Arg Glu 1825 1830 1835 tgg gtg ttg gac agt gta gca ctc tac cag tgc cag gag ctg gac acc 5691 Trp Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu Asp Thr 1840 1845 1850 tac ctg ata ccc cag atc ccc cac agc cac tac tga ctgcagccag 5737 Tyr Leu Ile Pro Gln Ile Pro His Ser His Tyr 1855 1860 ccacaggtac aggccacagg accccaagaa tgagcttaca aagtggcctt tccaggccct 5797 gggagctcct ctcactcttc agtccttcta ctgtcctggc tactaaatat tttatgtaca 5857 tcagcctgaa aaggacttct ggctatgcaa gggtccctta aagattttct gcttgaagtc 5917 tcccttggaa atctgccatg agcacaaaat tatggtaatt tttcacctga gaagatttta 5977 aaaccattta aacgccacca attgagcaag atgctgattc attatttatc agccctattc 6037 tttctattca ggctgttgtt ggcttagggc tggaagcaca gagtggcttg gcctcaagag 6097 aatagctggt ttccctaagt ttacttctct aaaaccctgt gttcacaaag gcagagagtc 6157 agacccttca atggaaggag agtgcttggg atcgattatg tgacttaaag tcagaatagt 6217 ccttgggcag ttctcaaatg ttggagtgga acattgggga ggaaattctg aggcaggtat 6277 tagaaatgaa aaggaaactt gaaacctggg catggtggct cacgcctgta atcccagcac 6337 tttgggaggc caaggtgggc agatcactgg aggtcaggag ttcgaaacca gcctggccaa 6397 catggtgaaa ccccatctct actaaaaata cagaaattag ccggtcatgg tggtggacac 6457 ctgtaatccc agctactcag gtggctaagg caggagaatc acttcagccc gggaggtgga 6517 ggttgcagtg agccaagatc ataccacggc actccagcct gggtgacagt gagactgtgg 6577 ctcaaaaaaa aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa agtctgagat 6637 atatttgcta gatttctaaa gaatgtgttc taaaacagca gaagattttc aagaaccggt 6697 ttccaaagac agtcttctaa ttcctcatta gtaataagta aaatgtttat tgttgtagct 6757 ctggtatata atccattcct cttaaaatat aagacctctg gcatgaatat ttcatatcta 6817 taaaatgaca gatcccacca ggaaggaagc tgttgctttc tttgaggtga tttttttcct 6877 ttgctccctg ttgctgaaac catacagctt cataaataat tttgcttgct gaaggaagaa 6937 aaagtgtttt tcataaaccc attatccagg actgtttata gctgttggaa ggactaggtc 6997 ttccctagcc cccccagtgt gcaagggcag tgaagacttg attgtacaaa atacgttttg 7057 taaatgttgt gctgttaaca ctgcaaataa acttggtagc aaaca 7102 14 6419 DNA H. sapiens CDS (341)...(5044) 14 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agctgcttgt gaattttctg agacggatgt aacaaatact gaacatcatc aacccagtaa 180 taatgatttg aacaccactg agaagcgtgc agctgagagg catccagaaa agtatcaggg 240 tagttctgtt tcaaacttgc atgtggagcc atgtggcaca aatactcatg ccagctcatt 300 acagcatgag aacagcagtt tattactcac taaagacaga atg aat gta gaa aag 355 Met Asn Val Glu Lys 1 5 gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca agg agc caa 403 Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala Arg Ser Gln 10 15 20 cat aac aga tgg gct gga agt aag gaa aca tgt aat gat agg cgg act 451 His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp Arg Arg Thr 25 30 35 ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc ctg tgt gag 499 Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro Leu Cys Glu 40 45 50 aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag aat cct aga 547 Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu Asn Pro Arg 55 60 65 gat act gaa gat gtt cct tgg ata aca cta aat agc agc att cag aaa 595 Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser Ile Gln Lys 70 75 80 85 gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt tct gat gac 643 Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly Ser Asp Asp 90 95 100 tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct gat gta ttg 691 Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala Asp Val Leu 105 110 115 gac gtt cta aat gag gta gat gaa tat tct ggt tct tca gag aaa ata 739 Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser Glu Lys Ile 120 125 130 gac tta ctg gcc agt gat cct cat gag gct tta ata tgt aaa agt gaa 787 Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys Lys Ser Glu 135 140 145 aga gtt cac tcc aaa tca gta gag agt aat att gaa gac aaa ata ttt 835 Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp Lys Ile Phe 150 155 160 165 ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta agc cat gta 883 Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu Ser His Val 170 175 180 act gaa aat cta att ata gga gca ttt gtt act gag cca cag ata ata 931 Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro Gln Ile Ile 185 190 195 caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg aga cct aca 979 Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg Arg Pro Thr 200 205 210 tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat ttg gca gtt 1027 Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp Leu Ala Val 215 220 225 caa aag act cct gaa atg ata aat cag gga act aac caa acg gag cag 1075 Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln Thr Glu Gln 230 235 240 245 aat ggt caa gtg atg aat att act aat agt ggt cat gag aat aaa aca 1123 Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu Asn Lys Thr 250 255 260 aaa ggt gat tct att cag aat gag aaa aat cct aac cca ata gaa tca 1171 Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro Ile Glu Ser 265 270 275 ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct ata agc agc 1219 Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro Ile Ser Ser 280 285 290 agt ata agc aat atg gaa ctc gaa tta aat atc cac aat tca aaa gca 1267 Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn Ser Lys Ala 295 300 305 cct aaa aag aat agg ctg agg agg aag tct tct acc agg cat att cat 1315 Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg His Ile His 310 315 320 325 gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct aat tgt act 1363 Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro Asn Cys Thr 330 335 340 gaa ttg caa att gat agt tgt tct agc agt gaa gag ata aag aaa aaa 1411 Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile Lys Lys Lys 345 350 355 aag tac aac caa atg cca gtc agg cac agc aga aac cta caa ctc atg 1459 Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu Gln Leu Met 360 365 370 gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac aag cca aat 1507 Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn Lys Pro Asn 375 380 385 gaa cag aca agt aaa aga cat gac agc gat act ttc cca gag ctg aag 1555 Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro Glu Leu Lys 390 395 400 405 tta aca aat gca cct ggt tct ttt act aag tgt tca aat acc agt gaa 1603 Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn Thr Ser Glu 410 415 420 ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa aaa gaa gag 1651 Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu Lys Glu Glu 425 430 435 aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac ccc aaa gat 1699 Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp Pro Lys Asp 440 445 450 ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga tct gta gag 1747 Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg Ser Val Glu 455 460 465 agt agc agt att tca ttg gta cct ggt act gat tat ggc act cag gaa 1795 Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly Thr Gln Glu 470 475 480 485 agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca aaa aca gaa 1843 Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala Lys Thr Glu 490 495 500 cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac ccc aag gga 1891 Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn Pro Lys Gly 505 510 515 cta att cat ggt tgt tcc aaa gat aat aga aat gac aca gaa ggc ttt 1939 Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr Glu Gly Phe 520 525 530 aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa aca agc ata 1987 Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu Thr Ser Ile 535 540 545 gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag aat aca ttc 2035 Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln Asn Thr Phe 550 555 560 565 aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat cca gga aat 2083 Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn Pro Gly Asn 570 575 580 gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg tcc tta aag 2131 Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly Ser Leu Lys 585 590 595 aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag gaa gaa aat 2179 Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys Glu Glu Asn 600 605 610 caa gga aag aat gag tct aat atc aag cct gta cag aca gtt aat atc 2227 Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr Val Asn Ile 615 620 625 act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca gtt gat aat 2275 Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro Val Asp Asn 630 635 640 645 gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta tca tct cag 2323 Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu Ser Ser Gln 650 655 660 ttc aga ggc aac gaa act gga ctc att act cca aat aaa cat gga ctt 2371 Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys His Gly Leu 665 670 675 tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc aag tca ttt 2419 Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile Lys Ser Phe 680 685 690 gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac ttt gag gaa 2467 Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn Phe Glu Glu 695 700 705 cat tca atg tca cct gaa aga gaa atg gga aat gag aac att cca agt 2515 His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn Ile Pro Ser 710 715 720 725 aca gtg agc aca att agc cgt aat aac att aga gaa aat gtt ttt aaa 2563 Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn Val Phe Lys 730 735 740 gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt act aat gaa 2611 Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser Thr Asn Glu 745 750 755 gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa aac att caa 2659 Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu Asn Ile Gln 760 765 770 gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct atg ctt aga 2707 Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala Met Leu Arg 775 780 785 tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt cct gga agt 2755 Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu Pro Gly Ser 790 795 800 805 aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa gaa gta gtt 2803 Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu Glu Val Val 810 815 820 cag act gtt aat aca gat ttc tct cca tat ctg att tca gat aac tta 2851 Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser Asp Asn Leu 825 830 835 gaa cag cct atg gga agt agt cat gca tct cag gtt tgt tct gag aca 2899 Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys Ser Glu Thr 840 845 850 cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat act agt ttt 2947 Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp Thr Ser Phe 855 860 865 gct gaa aat gac att aag gaa agt tct gct gtt ttt agc aaa agc gtc 2995 Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser Lys Ser Val 870 875 880 885 cag aaa gga gag ctt agc agg agt cct agc cct ttc acc cat aca cat 3043 Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr His Thr His 890 895 900 ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag tcc tca gaa 3091 Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu Ser Ser Glu 905 910 915 gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc caa cac ttg 3139 Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe Gln His Leu 920 925 930 tta ttt ggt aaa gta aac aat ata cct tct cag tct act agg cat agc 3187 Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr Arg His Ser 935 940 945 acc gtt gct acc gag tgt ctg tct aag aac aca gag gag aat tta tta 3235 Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu Asn Leu Leu 950 955 960 965 tca ttg aag aat agc tta aat gac tgc agt aac cag gta ata ttg gca 3283 Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val Ile Leu Ala 970 975 980 aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa tgt tct gct 3331 Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys Cys Ser Ala 985 990 995 agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg act gca aat 3379 Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu Thr Ala Asn 1000 1005 1010 aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa caa atg agg 3427 Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys Gln Met Arg 1015 1020 1025 cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag gaa ttg gtt 3475 His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys Glu Leu Val 1030 1035 1040 1045 tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat aat caa gaa 3523 Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn Asn Gln Glu 1050 1055 1060 gag caa agc atg gat tca aac tta ggt gaa gca gca tct ggg tgt gag 3571 Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser Gly Cys Glu 1065 1070 1075 agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc tct cag agt 3619 Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Ser Gln Ser 1080 1085 1090 gac att tta acc act cag cag agg gat acc atg caa cat aac ctg ata 3667 Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His Asn Leu Ile 1095 1100 1105 aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta gaa cag cat 3715 Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu Glu Gln His 1110 1115 1120 1125 ggg agc cag cct tct aac agc tac cct tcc atc ata agt gac tct tct 3763 Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser Asp Ser Ser 1130 1135 1140 gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca gaa aaa gca 3811 Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Glu Lys Ala 1145 1150 1155 gta tta act tca cag aaa agt agt gaa tac cct ata agc cag aat cca 3859 Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gln Asn Pro 1160 1165 1170 gaa ggc ctt tct gct gac aag ttt gag gtg tct gca gat agt tct acc 3907 Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Ser Ser Thr 1175 1180 1185 agt aaa aat aaa gaa cca gga gtg gaa agg tca tcc cct tct aaa tgc 3955 Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Ser Lys Cys 1190 1195 1200 1205 cca tca tta gat gat agg tgg tac atg cac agt tgc tct ggg agt ctt 4003 Pro Ser Leu Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gly Ser Leu 1210 1215 1220 cag aat aga aac tac cca tct caa gag gag ctc att aag gtt gtt gat 4051 Gln Asn Arg Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys Val Val Asp 1225 1230 1235 gtg gag gag caa cag ctg gaa gag tct ggg cca cac gat ttg acg gaa 4099 Val Glu Glu Gln Gln Leu Glu Glu Ser Gly Pro His Asp Leu Thr Glu 1240 1245 1250 aca tct tac ttg cca agg caa gat cta gag gga acc cct tac ctg gaa 4147 Thr Ser Tyr Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Tyr Leu Glu 1255 1260 1265 tct gga atc agc ctc ttc tct gat gac cct gaa tct gat cct tct gaa 4195 Ser Gly Ile Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pro Ser Glu 1270 1275 1280 1285 gac aga gcc cca gag tca gct cgt gtt ggc aac ata cca tct tca acc 4243 Asp Arg Ala Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Ser Ser Thr 1290 1295 1300 tct gca ttg aaa gtt ccc caa ttg aaa gtt gca gaa tct gcc cag agt 4291 Ser Ala Leu Lys Val Pro Gln Leu Lys Val Ala Glu Ser Ala Gln Ser 1305 1310 1315 cca gct gct gct cat act act gat act gct ggg tat aat gca atg gaa 4339 Pro Ala Ala Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Ala Met Glu 1320 1325 1330 gaa agt gtg agc agg gag aag cca gaa ttg aca gct tca aca gaa agg 4387 Glu Ser Val Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Thr Glu Arg 1335 1340 1345 gtc aac aaa aga atg tcc atg gtg gtg tct ggc ctg acc cca gaa gaa 4435 Val Asn Lys Arg Met Ser Met Val Val Ser Gly Leu Thr Pro Glu Glu 1350 1355 1360 1365 ttt atg ctc gtg tac aag ttt gcc aga aaa cac cac atc act tta act 4483 Phe Met Leu Val Tyr Lys Phe Ala Arg Lys His His Ile Thr Leu Thr 1370 1375 1380 aat cta att act gaa gag act act cat gtt gtt atg aaa aca gat gct 4531 Asn Leu Ile Thr Glu Glu Thr Thr His Val Val Met Lys Thr Asp Ala 1385 1390 1395 gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta gga att gcg gga 4579 Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Ile Ala Gly 1400 1405 1410 gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag tct att aaa gaa 4627 Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln Ser Ile Lys Glu 1415 1420 1425 aga aaa atg ctg aat gag cat gat ttt gaa gtc aga gga gat gtg gtc 4675 Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg Gly Asp Val Val 1430 1435 1440 1445 aat gga aga aac cac caa ggt cca aag cga gca aga gaa tcc cag gac 4723 Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg Glu Ser Gln Asp 1450 1455 1460 aga aag atc ttc agg ggg cta gaa atc tgt tgc tat ggg ccc ttc acc 4771 Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pro Phe Thr 1465 1470 1475 aac atg ccc aca gat caa ctg gaa tgg atg gta cag ctg tgt ggt gct 4819 Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cys Gly Ala 1480 1485 1490 tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc aca ggt gtc cac 4867 Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gly Val His 1495 1500 1505 cca att gtg gtt gtg cag cca gat gcc tgg aca gag gac aat ggc ttc 4915 Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu Asp Asn Gly Phe 1510 1515 1520 1525 cat gca att ggg cag atg tgt gag gca cct gtg gtg acc cga gag tgg 4963 His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val Thr Arg Glu Trp 1530 1535 1540 gtg ttg gac agt gta gca ctc tac cag tgc cag gag ctg gac acc tac 5011 Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr 1545 1550 1555 ctg ata ccc cag atc ccc cac agc cac tac tga ctgcagccag ccacaggtac 5064 Leu Ile Pro Gln Ile Pro His Ser His Tyr 1560 1565 agagcacagg accccaagaa tgagcttaca aagtggcctt tccaggccct gggagctcct 5124 ctcactcttc agtccttcta ctgtcctggc tactaaatat tttatgtaca tcagcctgaa 5184 aaggacttct ggctatgcaa gggtccctta aagattttct gcttgaagtc tcccttggaa 5244 atctgccatg agcacaaaat tatggtaatt tttcacctga gaagatttta aaaccattta 5304 aacgccacca attgagcaag atgctgattc attatttatc agccctattc tttctattca 5364 ggctgttgtt ggcttagggc tggaagcaca gagtggcttg gcctcaagag aatagctggt 5424 ttccctaagt ttacttctct aaaaccctgt gttcacaaag gcagagagtc agacccttca 5484 atggaaggag agtgcttggg atcgattatg tgacttaaag tcagaatagt ccttgggcag 5544 ttctcaaatg ttggagtgga acattgggga ggaaattctg aggcaggtat tagaaatgaa 5604 aaggaaactt gaaacctggg catggtggct cacgcctgta atcccagcac tttgggaggc 5664 caaggtgggc agatcactgg aggtcaggag ttcgaaacca gcctggccaa catggtgaaa 5724 ccccatctct actaaaaata cagaaattag ccggtcatgg tggtggacac ctgtaatccc 5784 agctactcag gtggctaagg caggagaatc acttcagccc gggaggtgga ggttgcagtg 5844 agccaagatc ataccacggc actccagcct gggtgacagt gagactgtgg ctcaaaaaaa 5904 aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa agtctgagat atatttgcta 5964 gatttctaaa gaatgtgttc taaaacagca gaagattttc aagaaccggt ttccaaagac 6024 agtcttctaa ttcctcatta gtaataagta aaatgtttat tgttgtagct ctggtatata 6084 atccattcct cttaaaatat aagacctctg gcatgaatat ttcatatcta taaaatgaca 6144 gatcccacca ggaaggaagc tgttgctttc tttgaggtga tttttttcct ttgctccctg 6204 ttgctgaaac catacagctt cataaataat tttgcttgct gaaggaagaa aaagtgtttt 6264 tcataaaccc attatccagg actgtttata gctgttggaa ggactaggtc ttccctagcc 6324 cccccagtgt gcaagggcag tgaagacttg attgtacaaa atacgttttg taaatgttgt 6384 gctgttaaca ctgcaaataa acttggtagc aaaca 6419 15 3559 DNA H. sapiens CDS (142)...(2184) 15 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg ggt gaa gca gca 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Glu Ala Ala 175 180 185 tct ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta 747 Ser Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu 190 195 200 tcc tct cag agt gac att tta acc act cag cag agg gat acc atg caa 795 Ser Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln 205 210 215 cat aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg 843 His Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val 220 225 230 tta gaa cag cat ggg agc cag cct tct aac agc tac cct tcc atc ata 891 Leu Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile 235 240 245 250 agt gac tct tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca 939 Ser Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr 255 260 265 tca gaa aaa gca gta tta act tca cag aaa agt agt gaa tac cct ata 987 Ser Glu Lys Ala Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile 270 275 280 agc cag aat cca gaa ggc ctt tct gct gac aag ttt gag gtg tct gca 1035 Ser Gln Asn Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala 285 290 295 gat agt tct acc agt aaa aat aaa gaa cca gga gtg gaa agg tca tcc 1083 Asp Ser Ser Thr Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Ser Ser 300 305 310 cct tct aaa tgc cca tca tta gat gat agg tgg tac atg cac agt tgc 1131 Pro Ser Lys Cys Pro Ser Leu Asp Asp Arg Trp Tyr Met His Ser Cys 315 320 325 330 tct ggg agt ctt cag aat aga aac tac cca tct caa gag gag ctc att 1179 Ser Gly Ser Leu Gln Asn Arg Asn Tyr Pro Ser Gln Glu Glu Leu Ile 335 340 345 aag gtt gtt gat gtg gag gag caa cag ctg gaa gag tct ggg cca cac 1227 Lys Val Val Asp Val Glu Glu Gln Gln Leu Glu Glu Ser Gly Pro His 350 355 360 gat ttg acg gaa aca tct tac ttg cca agg caa gat cta gag gga acc 1275 Asp Leu Thr Glu Thr Ser Tyr Leu Pro Arg Gln Asp Leu Glu Gly Thr 365 370 375 cct tac ctg gaa tct gga atc agc ctc ttc tct gat gac cct gaa tct 1323 Pro Tyr Leu Glu Ser Gly Ile Ser Leu Phe Ser Asp Asp Pro Glu Ser 380 385 390 gat cct tct gaa gac aga gcc cca gag tca gct cgt gtt ggc aac ata 1371 Asp Pro Ser Glu Asp Arg Ala Pro Glu Ser Ala Arg Val Gly Asn Ile 395 400 405 410 cca tct tca acc tct gca ttg aaa gtt ccc caa ttg aaa gtt gca gaa 1419 Pro Ser Ser Thr Ser Ala Leu Lys Val Pro Gln Leu Lys Val Ala Glu 415 420 425 tct gcc cag agt cca gct gct gct cat act act gat act gct ggg tat 1467 Ser Ala Gln Ser Pro Ala Ala Ala His Thr Thr Asp Thr Ala Gly Tyr 430 435 440 aat gca atg gaa gaa agt gtg agc agg gag aag cca gaa ttg aca gct 1515 Asn Ala Met Glu Glu Ser Val Ser Arg Glu Lys Pro Glu Leu Thr Ala 445 450 455 tca aca gaa agg gtc aac aaa aga atg tcc atg gtg gtg tct ggc ctg 1563 Ser Thr Glu Arg Val Asn Lys Arg Met Ser Met Val Val Ser Gly Leu 460 465 470 acc cca gaa gaa ttt atg ctc gtg tac aag ttt gcc aga aaa cac cac 1611 Thr Pro Glu Glu Phe Met Leu Val Tyr Lys Phe Ala Arg Lys His His 475 480 485 490 atc act tta act aat cta att act gaa gag act act cat gtt gtt atg 1659 Ile Thr Leu Thr Asn Leu Ile Thr Glu Glu Thr Thr His Val Val Met 495 500 505 aaa aca gat gct gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta 1707 Lys Thr Asp Ala Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu 510 515 520 gga att gcg gga gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag 1755 Gly Ile Ala Gly Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln 525 530 535 tct att aaa gaa aga aaa atg ctg aat gag cat gat ttt gaa gtc aga 1803 Ser Ile Lys Glu Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg 540 545 550 gga gat gtg gtc aat gga aga aac cac caa ggt cca aag cga gca aga 1851 Gly Asp Val Val Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg 555 560 565 570 gaa tcc cag gac aga aag atc ttc agg ggg cta gaa atc tgt tgc tat 1899 Glu Ser Gln Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr 575 580 585 ggg ccc ttc acc aac atg ccc aca gat caa ctg gaa tgg atg gta cag 1947 Gly Pro Phe Thr Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln 590 595 600 ctg tgt ggt gct tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc 1995 Leu Cys Gly Ala Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly 605 610 615 aca ggt gtc cac cca att gtg gtt gtg cag cca gat gcc tgg aca gag 2043 Thr Gly Val His Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu 620 625 630 gac aat ggc ttc cat gca att ggg cag atg tgt gag gca cct gtg gtg 2091 Asp Asn Gly Phe His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val 635 640 645 650 acc cga gag tgg gtg ttg gac agt gta gca ctc tac cag tgc cag gag 2139 Thr Arg Glu Trp Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu 655 660 665 ctg gac acc tac ctg ata ccc cag atc ccc cac agc cac tac tga 2184 Leu Asp Thr Tyr Leu Ile Pro Gln Ile Pro His Ser His Tyr 670 675 680 ctgcagccag ccacaggtac agagcacagg accccaagaa tgagcttaca aagtggcctt 2244 tccaggccct gggagctcct ctcactcttc agtccttcta ctgtcctggc tactaaatat 2304 tttatgtaca tcagcctgaa aaggacttct ggctatgcaa gggtccctta aagattttct 2364 gcttgaagtc tcccttggaa atctgccatg agcacaaaat tatggtaatt tttcacctga 2424 gaagatttta aaaccattta aacgccacca attgagcaag atgctgattc attatttatc 2484 agccctattc tttctattca ggctgttgtt ggcttagggc tggaagcaca gagtggcttg 2544 gcctcaagag aatagctggt ttccctaagt ttacttctct aaaaccctgt gttcacaaag 2604 gcagagagtc agacccttca atggaaggag agtgcttggg atcgattatg tgacttaaag 2664 tcagaatagt ccttgggcag ttctcaaatg ttggagtgga acattgggga ggaaattctg 2724 aggcaggtat tagaaatgaa aaggaaactt gaaacctggg catggtggct cacgcctgta 2784 atcccagcac tttgggaggc caaggtgggc agatcactgg aggtcaggag ttcgaaacca 2844 gcctggccaa catggtgaaa ccccatctct actaaaaata cagaaattag ccggtcatgg 2904 tggtggacac ctgtaatccc agctactcag gtggctaagg caggagaatc acttcagccc 2964 gggaggtgga ggttgcagtg agccaagatc ataccacggc actccagcct gggtgacagt 3024 gagactgtgg ctcaaaaaaa aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa 3084 agtctgagat atatttgcta gatttctaaa gaatgtgttc taaaacagca gaagattttc 3144 aagaaccggt ttccaaagac agtcttctaa ttcctcatta gtaataagta aaatgtttat 3204 tgttgtagct ctggtatata atccattcct cttaaaatat aagacctctg gcatgaatat 3264 ttcatatcta taaaatgaca gatcccacca ggaaggaagc tgttgctttc tttgaggtga 3324 tttttttcct ttgctccctg ttgctgaaac catacagctt cataaataat tttgcttgct 3384 gaaggaagaa aaagtgtttt tcataaaccc attatccagg actgtttata gctgttggaa 3444 ggactaggtc ttccctagcc cccccagtgt gcaagggcag tgaagacttg attgtacaaa 3504 atacgttttg taaatgttgt gctgttaaca ctgcaaataa acttggtagc aaaca 3559 16 6391 DNA H. sapiens CDS (142)...(5016) 16 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca 843 Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr 220 225 230 aat act gaa cat cat caa ccc agt aat aat gat ttg aac acc act gag 891 Asn Thr Glu His His Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu 235 240 245 250 aag cgt gca gct gag agg cat cca gaa aag tat cag ggt agt tct gtt 939 Lys Arg Ala Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Ser Ser Val 255 260 265 tca aac ttg cat gtg gag cca tgt ggc aca aat act cat gcc agc tca 987 Ser Asn Leu His Val Glu Pro Cys Gly Thr Asn Thr His Ala Ser Ser 270 275 280 tta cag cat gag aac agc agt tta tta ctc act aaa gac aga atg aat 1035 Leu Gln His Glu Asn Ser Ser Leu Leu Leu Thr Lys Asp Arg Met Asn 285 290 295 gta gaa aag gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca 1083 Val Glu Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala 300 305 310 agg agc caa cat aac aga tgg gct gga agt aag gaa aca tgt aat gat 1131 Arg Ser Gln His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp 315 320 325 330 agg cgg act ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc 1179 Arg Arg Thr Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro 335 340 345 ctg tgt gag aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag 1227 Leu Cys Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu 350 355 360 aat cct aga gat act gaa gat gtt cct tgg ata aca cta aat agc agc 1275 Asn Pro Arg Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser 365 370 375 att cag aaa gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt 1323 Ile Gln Lys Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly 380 385 390 tct gat gac tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct 1371 Ser Asp Asp Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala 395 400 405 410 gat gta ttg gac gtt cta aat gag gta gat gaa tat tct ggt tct tca 1419 Asp Val Leu Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser 415 420 425 gag aaa ata gac tta ctg gcc agt gat cct cat gag gct tta ata tgt 1467 Glu Lys Ile Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys 430 435 440 aaa agt gaa aga gtt cac tcc aaa tca gta gag agt aat att gaa gac 1515 Lys Ser Glu Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp 445 450 455 aaa ata ttt ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta 1563 Lys Ile Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu 460 465 470 agc cat gta act gaa aat cta att ata gga gca ttt gtt act gag cca 1611 Ser His Val Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro 475 480 485 490 cag ata ata caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg 1659 Gln Ile Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg 495 500 505 aga cct aca tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat 1707 Arg Pro Thr Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp 510 515 520 ttg gca gtt caa aag act cct gaa atg ata aat cag gga act aac caa 1755 Leu Ala Val Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln 525 530 535 acg gag cag aat ggt caa gtg atg aat att act aat agt ggt cat gag 1803 Thr Glu Gln Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu 540 545 550 aat aaa aca aaa ggt gat tct att cag aat gag aaa aat cct aac cca 1851 Asn Lys Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro 555 560 565 570 ata gaa tca ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct 1899 Ile Glu Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro 575 580 585 ata agc agc agt ata agc aat atg gaa ctc gaa tta aat atc cac aat 1947 Ile Ser Ser Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn 590 595 600 tca aaa gca cct aaa aag aat agg ctg agg agg aag tct tct acc agg 1995 Ser Lys Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg 605 610 615 cat att cat gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct 2043 His Ile His Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro 620 625 630 aat tgt act gaa ttg caa att gat agt tgt tct agc agt gaa gag ata 2091 Asn Cys Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile 635 640 645 650 aag aaa aaa aag tac aac caa atg cca gtc agg cac agc aga aac cta 2139 Lys Lys Lys Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu 655 660 665 caa ctc atg gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac 2187 Gln Leu Met Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn 670 675 680 aag cca aat gaa cag aca agt aaa aga cat gac agc gat act ttc cca 2235 Lys Pro Asn Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro 685 690 695 gag ctg aag tta aca aat gca cct ggt tct ttt act aag tgt tca aat 2283 Glu Leu Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn 700 705 710 acc agt gaa ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa 2331 Thr Ser Glu Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu 715 720 725 730 aaa gaa gag aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac 2379 Lys Glu Glu Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp 735 740 745 ccc aaa gat ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga 2427 Pro Lys Asp Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg 750 755 760 tct gta gag agt agc agt att tca ttg gta cct ggt act gat tat ggc 2475 Ser Val Glu Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly 765 770 775 act cag gaa agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca 2523 Thr Gln Glu Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala 780 785 790 aaa aca gaa cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac 2571 Lys Thr Glu Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn 795 800 805 810 ccc aag gga cta att cat ggt tgt tcc aaa gat aat aga aat gac aca 2619 Pro Lys Gly Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr 815 820 825 gaa ggc ttt aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa 2667 Glu Gly Phe Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu 830 835 840 aca agc ata gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag 2715 Thr Ser Ile Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln 845 850 855 aat aca ttc aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat 2763 Asn Thr Phe Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn 860 865 870 cca gga aat gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg 2811 Pro Gly Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly 875 880 885 890 tcc tta aag aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag 2859 Ser Leu Lys Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys 895 900 905 gaa gaa aat caa gga aag aat gag tct aat atc aag cct gta cag aca 2907 Glu Glu Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr 910 915 920 gtt aat atc act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca 2955 Val Asn Ile Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro 925 930 935 gtt gat aat gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta 3003 Val Asp Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu 940 945 950 tca tct cag ttc aga ggc aac gaa act gga ctc att act cca aat aaa 3051 Ser Ser Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys 955 960 965 970 cat gga ctt tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc 3099 His Gly Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile 975 980 985 aag tca ttt gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac 3147 Lys Ser Phe Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn 990 995 1000 ttt gag gaa cat tca atg tca cct gaa aga gaa atg gga aat gag aac 3195 Phe Glu Glu His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn 1005 1010 1015 att cca agt aca gtg agc aca att agc cgt aat aac att aga gaa aat 3243 Ile Pro Ser Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn 1020 1025 1030 gtt ttt aaa gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt 3291 Val Phe Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser 1035 1040 1045 1050 act aat gaa gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa 3339 Thr Asn Glu Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu 1055 1060 1065 aac att caa gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct 3387 Asn Ile Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala 1070 1075 1080 atg ctt aga tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt 3435 Met Leu Arg Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu 1085 1090 1095 cct gga agt aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa 3483 Pro Gly Ser Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu 1100 1105 1110 gaa gta gtt cag act gtt aat aca gat ttc tct cca tat ctg att tca 3531 Glu Val Val Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser 1115 1120 1125 1130 gat aac tta gaa cag cct atg gga agt agt cat gca tct cag gtt tgt 3579 Asp Asn Leu Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys 1135 1140 1145 tct gag aca cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat 3627 Ser Glu Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp 1150 1155 1160 act agt ttt gct gaa aat gac att aag gaa agt tct gct gtt ttt agc 3675 Thr Ser Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser 1165 1170 1175 aaa agc gtc cag aaa gga gag ctt agc agg agt cct agc cct ttc acc 3723 Lys Ser Val Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr 1180 1185 1190 cat aca cat ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag 3771 His Thr His Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu 1195 1200 1205 1210 tcc tca gaa gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc 3819 Ser Ser Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe 1215 1220 1225 caa cac ttg tta ttt ggt aaa gta aac aat ata cct tct cag tct act 3867 Gln His Leu Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr 1230 1235 1240 agg cat agc acc gtt gct acc gag tgt ctg tct aag aac aca gag gag 3915 Arg His Ser Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu 1245 1250 1255 aat tta tta tca ttg aag aat agc tta aat gac tgc agt aac cag gta 3963 Asn Leu Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val 1260 1265 1270 ata ttg gca aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa 4011 Ile Leu Ala Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys 1275 1280 1285 1290 tgt tct gct agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg 4059 Cys Ser Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu 1295 1300 1305 act gca aat aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa 4107 Thr Ala Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys 1310 1315 1320 caa atg agg cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag 4155 Gln Met Arg His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys 1325 1330 1335 gaa ttg gtt tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat 4203 Glu Leu Val Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn 1340 1345 1350 aat caa gaa gag caa agc atg gat tca aac tta ggt gaa gca gca tct 4251 Asn Gln Glu Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser 1355 1360 1365 1370 ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc 4299 Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser 1375 1380 1385 tct cag agt gac att tta acc act cag cag agg gat acc atg caa cat 4347 Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His 1390 1395 1400 aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta 4395 Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu 1405 1410 1415 gaa cag cat ggg agc cag cct tct aac agc tac cct tcc atc ata agt 4443 Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser 1420 1425 1430 gac tct tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca 4491 Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser 1435 1440 1445 1450 gaa aaa gat gct gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta 4539 Glu Lys Asp Ala Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu 1455 1460 1465 gga att gcg gga gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag 4587 Gly Ile Ala Gly Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln 1470 1475 1480 tct att aaa gaa aga aaa atg ctg aat gag cat gat ttt gaa gtc aga 4635 Ser Ile Lys Glu Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg 1485 1490 1495 gga gat gtg gtc aat gga aga aac cac caa ggt cca aag cga gca aga 4683 Gly Asp Val Val Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg 1500 1505 1510 gaa tcc cag gac aga aag atc ttc agg ggg cta gaa atc tgt tgc tat 4731 Glu Ser Gln Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr 1515 1520 1525 1530 ggg ccc ttc acc aac atg ccc aca gat caa ctg gaa tgg atg gta cag 4779 Gly Pro Phe Thr Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln 1535 1540 1545 ctg tgt ggt gct tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc 4827 Leu Cys Gly Ala Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly 1550 1555 1560 aca ggt gtc cac cca att gtg gtt gtg cag cca gat gcc tgg aca gag 4875 Thr Gly Val His Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu 1565 1570 1575 gac aat ggc ttc cat gca att ggg cag atg tgt gag gca cct gtg gtg 4923 Asp Asn Gly Phe His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val 1580 1585 1590 acc cga gag tgg gtg ttg gac agt gta gca ctc tac cag tgc cag gag 4971 Thr Arg Glu Trp Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu 1595 1600 1605 1610 ctg gac acc tac ctg ata ccc cag atc ccc cac agc cac tac tga 5016 Leu Asp Thr Tyr Leu Ile Pro Gln Ile Pro His Ser His Tyr 1615 1620 ctgcagccag ccacaggtac agaccacagg accccaagaa tgagcttaca aagtggcctt 5076 tccaggccct gggagctcct ctcactcttc agtccttcta ctgtcctggc tactaaatat 5136 tttatgtaca tcagcctgaa aaggacttct ggctatgcaa gggtccctta aagattttct 5196 gcttgaagtc tcccttggaa atctgccatg agcacaaaat tatggtaatt tttcacctga 5256 gaagatttta aaaccattta aacgccacca attgagcaag atgctgattc attatttatc 5316 agccctattc tttctattca ggctgttgtt ggcttagggc tggaagcaca gagtggcttg 5376 gcctcaagag aatagctggt ttccctaagt ttacttctct aaaaccctgt gttcacaaag 5436 gcagagagtc agacccttca atggaaggag agtgcttggg atcgattatg tgacttaaag 5496 tcagaatagt ccttgggcag ttctcaaatg ttggagtgga acattgggga ggaaattctg 5556 aggcaggtat tagaaatgaa aaggaaactt gaaacctggg catggtggct cacgcctgta 5616 atcccagcac tttgggaggc caaggtgggc agatcactgg aggtcaggag ttcgaaacca 5676 gcctggccaa catggtgaaa ccccatctct actaaaaata cagaaattag ccggtcatgg 5736 tggtggacac ctgtaatccc agctactcag gtggctaagg caggagaatc acttcagccc 5796 gggaggtgga ggttgcagtg agccaagatc ataccacggc actccagcct gggtgacagt 5856 gagactgtgg ctcaaaaaaa aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa 5916 agtctgagat atatttgcta gatttctaaa gaatgtgttc taaaacagca gaagattttc 5976 aagaaccggt ttccaaagac agtcttctaa ttcctcatta gtaataagta aaatgtttat 6036 tgttgtagct ctggtatata atccattcct cttaaaatat aagacctctg gcatgaatat 6096 ttcatatcta taaaatgaca gatcccacca ggaaggaagc tgttgctttc tttgaggtga 6156 tttttttcct ttgctccctg ttgctgaaac catacagctt cataaataat tttgcttgct 6216 gaaggaagaa aaagtgtttt tcataaaccc attatccagg actgtttata gctgttggaa 6276 ggactaggtc ttccctagcc cccccagtgt gcaagggcag tgaagacttg attgtacaaa 6336 atacgttttg taaatgttgt gctgttaaca ctgcaaataa acttggtagc aaaca 6391 17 6313 DNA H. sapiens CDS (142)...(4938) 17 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca 843 Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr 220 225 230 aat act gaa cat cat caa ccc agt aat aat gat ttg aac acc act gag 891 Asn Thr Glu His His Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu 235 240 245 250 aag cgt gca gct gag agg cat cca gaa aag tat cag ggt agt tct gtt 939 Lys Arg Ala Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Ser Ser Val 255 260 265 tca aac ttg cat gtg gag cca tgt ggc aca aat act cat gcc agc tca 987 Ser Asn Leu His Val Glu Pro Cys Gly Thr Asn Thr His Ala Ser Ser 270 275 280 tta cag cat gag aac agc agt tta tta ctc act aaa gac aga atg aat 1035 Leu Gln His Glu Asn Ser Ser Leu Leu Leu Thr Lys Asp Arg Met Asn 285 290 295 gta gaa aag gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca 1083 Val Glu Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala 300 305 310 agg agc caa cat aac aga tgg gct gga agt aag gaa aca tgt aat gat 1131 Arg Ser Gln His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp 315 320 325 330 agg cgg act ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc 1179 Arg Arg Thr Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro 335 340 345 ctg tgt gag aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag 1227 Leu Cys Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu 350 355 360 aat cct aga gat act gaa gat gtt cct tgg ata aca cta aat agc agc 1275 Asn Pro Arg Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser 365 370 375 att cag aaa gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt 1323 Ile Gln Lys Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly 380 385 390 tct gat gac tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct 1371 Ser Asp Asp Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala 395 400 405 410 gat gta ttg gac gtt cta aat gag gta gat gaa tat tct ggt tct tca 1419 Asp Val Leu Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser 415 420 425 gag aaa ata gac tta ctg gcc agt gat cct cat gag gct tta ata tgt 1467 Glu Lys Ile Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys 430 435 440 aaa agt gaa aga gtt cac tcc aaa tca gta gag agt aat att gaa gac 1515 Lys Ser Glu Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp 445 450 455 aaa ata ttt ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta 1563 Lys Ile Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu 460 465 470 agc cat gta act gaa aat cta att ata gga gca ttt gtt act gag cca 1611 Ser His Val Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro 475 480 485 490 cag ata ata caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg 1659 Gln Ile Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg 495 500 505 aga cct aca tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat 1707 Arg Pro Thr Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp 510 515 520 ttg gca gtt caa aag act cct gaa atg ata aat cag gga act aac caa 1755 Leu Ala Val Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln 525 530 535 acg gag cag aat ggt caa gtg atg aat att act aat agt ggt cat gag 1803 Thr Glu Gln Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu 540 545 550 aat aaa aca aaa ggt gat tct att cag aat gag aaa aat cct aac cca 1851 Asn Lys Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro 555 560 565 570 ata gaa tca ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct 1899 Ile Glu Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro 575 580 585 ata agc agc agt ata agc aat atg gaa ctc gaa tta aat atc cac aat 1947 Ile Ser Ser Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn 590 595 600 tca aaa gca cct aaa aag aat agg ctg agg agg aag tct tct acc agg 1995 Ser Lys Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg 605 610 615 cat att cat gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct 2043 His Ile His Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro 620 625 630 aat tgt act gaa ttg caa att gat agt tgt tct agc agt gaa gag ata 2091 Asn Cys Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile 635 640 645 650 aag aaa aaa aag tac aac caa atg cca gtc agg cac agc aga aac cta 2139 Lys Lys Lys Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu 655 660 665 caa ctc atg gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac 2187 Gln Leu Met Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn 670 675 680 aag cca aat gaa cag aca agt aaa aga cat gac agc gat act ttc cca 2235 Lys Pro Asn Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro 685 690 695 gag ctg aag tta aca aat gca cct ggt tct ttt act aag tgt tca aat 2283 Glu Leu Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn 700 705 710 acc agt gaa ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa 2331 Thr Ser Glu Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu 715 720 725 730 aaa gaa gag aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac 2379 Lys Glu Glu Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp 735 740 745 ccc aaa gat ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga 2427 Pro Lys Asp Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg 750 755 760 tct gta gag agt agc agt att tca ttg gta cct ggt act gat tat ggc 2475 Ser Val Glu Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly 765 770 775 act cag gaa agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca 2523 Thr Gln Glu Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala 780 785 790 aaa aca gaa cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac 2571 Lys Thr Glu Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn 795 800 805 810 ccc aag gga cta att cat ggt tgt tcc aaa gat aat aga aat gac aca 2619 Pro Lys Gly Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr 815 820 825 gaa ggc ttt aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa 2667 Glu Gly Phe Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu 830 835 840 aca agc ata gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag 2715 Thr Ser Ile Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln 845 850 855 aat aca ttc aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat 2763 Asn Thr Phe Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn 860 865 870 cca gga aat gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg 2811 Pro Gly Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly 875 880 885 890 tcc tta aag aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag 2859 Ser Leu Lys Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys 895 900 905 gaa gaa aat caa gga aag aat gag tct aat atc aag cct gta cag aca 2907 Glu Glu Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr 910 915 920 gtt aat atc act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca 2955 Val Asn Ile Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro 925 930 935 gtt gat aat gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta 3003 Val Asp Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu 940 945 950 tca tct cag ttc aga ggc aac gaa act gga ctc att act cca aat aaa 3051 Ser Ser Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys 955 960 965 970 cat gga ctt tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc 3099 His Gly Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile 975 980 985 aag tca ttt gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac 3147 Lys Ser Phe Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn 990 995 1000 ttt gag gaa cat tca atg tca cct gaa aga gaa atg gga aat gag aac 3195 Phe Glu Glu His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn 1005 1010 1015 att cca agt aca gtg agc aca att agc cgt aat aac att aga gaa aat 3243 Ile Pro Ser Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn 1020 1025 1030 gtt ttt aaa gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt 3291 Val Phe Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser 1035 1040 1045 1050 act aat gaa gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa 3339 Thr Asn Glu Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu 1055 1060 1065 aac att caa gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct 3387 Asn Ile Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala 1070 1075 1080 atg ctt aga tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt 3435 Met Leu Arg Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu 1085 1090 1095 cct gga agt aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa 3483 Pro Gly Ser Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu 1100 1105 1110 gaa gta gtt cag act gtt aat aca gat ttc tct cca tat ctg att tca 3531 Glu Val Val Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser 1115 1120 1125 1130 gat aac tta gaa cag cct atg gga agt agt cat gca tct cag gtt tgt 3579 Asp Asn Leu Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys 1135 1140 1145 tct gag aca cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat 3627 Ser Glu Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp 1150 1155 1160 act agt ttt gct gaa aat gac att aag gaa agt tct gct gtt ttt agc 3675 Thr Ser Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser 1165 1170 1175 aaa agc gtc cag aaa gga gag ctt agc agg agt cct agc cct ttc acc 3723 Lys Ser Val Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr 1180 1185 1190 cat aca cat ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag 3771 His Thr His Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu 1195 1200 1205 1210 tcc tca gaa gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc 3819 Ser Ser Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe 1215 1220 1225 caa cac ttg tta ttt ggt aaa gta aac aat ata cct tct cag tct act 3867 Gln His Leu Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr 1230 1235 1240 agg cat agc acc gtt gct acc gag tgt ctg tct aag aac aca gag gag 3915 Arg His Ser Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu 1245 1250 1255 aat tta tta tca ttg aag aat agc tta aat gac tgc agt aac cag gta 3963 Asn Leu Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val 1260 1265 1270 ata ttg gca aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa 4011 Ile Leu Ala Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys 1275 1280 1285 1290 tgt tct gct agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg 4059 Cys Ser Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu 1295 1300 1305 act gca aat aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa 4107 Thr Ala Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys 1310 1315 1320 caa atg agg cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag 4155 Gln Met Arg His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys 1325 1330 1335 gaa ttg gtt tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat 4203 Glu Leu Val Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn 1340 1345 1350 aat caa gaa gag caa agc atg gat tca aac tta ggt gaa gca gca tct 4251 Asn Gln Glu Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser 1355 1360 1365 1370 ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc 4299 Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser 1375 1380 1385 tct cag agt gac att tta acc act cag cag agg gat acc atg caa cat 4347 Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His 1390 1395 1400 aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta 4395 Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu 1405 1410 1415 gaa cag cat ggg agc cag cct tct aac agc tac cct tcc atc ata agt 4443 Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser 1420 1425 1430 gac tct tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca 4491 Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser 1435 1440 1445 1450 gaa aaa ggg gtg acc cag tct att aaa gaa aga aaa atg ctg aat gag 4539 Glu Lys Gly Val Thr Gln Ser Ile Lys Glu Arg Lys Met Leu Asn Glu 1455 1460 1465 cat gat ttt gaa gtc aga gga gat gtg gtc aat gga aga aac cac caa 4587 His Asp Phe Glu Val Arg Gly Asp Val Val Asn Gly Arg Asn His Gln 1470 1475 1480 ggt cca aag cga gca aga gaa tcc cag gac aga aag atc ttc agg ggg 4635 Gly Pro Lys Arg Ala Arg Glu Ser Gln Asp Arg Lys Ile Phe Arg Gly 1485 1490 1495 cta gaa atc tgt tgc tat ggg ccc ttc acc aac atg ccc aca gat caa 4683 Leu Glu Ile Cys Cys Tyr Gly Pro Phe Thr Asn Met Pro Thr Asp Gln 1500 1505 1510 ctg gaa tgg atg gta cag ctg tgt ggt gct tct gtg gtg aag gag ctt 4731 Leu Glu Trp Met Val Gln Leu Cys Gly Ala Ser Val Val Lys Glu Leu 1515 1520 1525 1530 tca tca ttc acc ctt ggc aca ggt gtc cac cca att gtg gtt gtg cag 4779 Ser Ser Phe Thr Leu Gly Thr Gly Val His Pro Ile Val Val Val Gln 1535 1540 1545 cca gat gcc tgg aca gag gac aat ggc ttc cat gca att ggg cag atg 4827 Pro Asp Ala Trp Thr Glu Asp Asn Gly Phe His Ala Ile Gly Gln Met 1550 1555 1560 tgt gag gca cct gtg gtg acc cga gag tgg gtg ttg gac agt gta gca 4875 Cys Glu Ala Pro Val Val Thr Arg Glu Trp Val Leu Asp Ser Val Ala 1565 1570 1575 ctc tac cag tgc cag gag ctg gac acc tac ctg ata ccc cag atc ccc 4923 Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Leu Ile Pro Gln Ile Pro 1580 1585 1590 cac agc cac tac tga ctgcagccag ccacaggtac aagccacagg accccaagaa 4978 His Ser His Tyr 1595 tgagcttaca aagtggcctt tccaggccct gggagctcct ctcactcttc agtccttcta 5038 ctgtcctggc tactaaatat tttatgtaca tcagcctgaa aaggacttct ggctatgcaa 5098 gggtccctta aagattttct gcttgaagtc tcccttggaa atctgccatg agcacaaaat 5158 tatggtaatt tttcacctga gaagatttta aaaccattta aacgccacca attgagcaag 5218 atgctgattc attatttatc agccctattc tttctattca ggctgttgtt ggcttagggc 5278 tggaagcaca gagtggcttg gcctcaagag aatagctggt ttccctaagt ttacttctct 5338 aaaaccctgt gttcacaaag gcagagagtc agacccttca atggaaggag agtgcttggg 5398 atcgattatg tgacttaaag tcagaatagt ccttgggcag ttctcaaatg ttggagtgga 5458 acattgggga ggaaattctg aggcaggtat tagaaatgaa aaggaaactt gaaacctggg 5518 catggtggct cacgcctgta atcccagcac tttgggaggc caaggtgggc agatcactgg 5578 aggtcaggag ttcgaaacca gcctggccaa catggtgaaa ccccatctct actaaaaata 5638 cagaaattag ccggtcatgg tggtggacac ctgtaatccc agctactcag gtggctaagg 5698 caggagaatc acttcagccc gggaggtgga ggttgcagtg agccaagatc ataccacggc 5758 actccagcct gggtgacagt gagactgtgg ctcaaaaaaa aaaaaaaaaa aggaaaatga 5818 aactaggaaa ggtttcttaa agtctgagat atatttgcta gatttctaaa gaatgtgttc 5878 taaaacagca gaagattttc aagaaccggt ttccaaagac agtcttctaa ttcctcatta 5938 gtaataagta aaatgtttat tgttgtagct ctggtatata atccattcct cttaaaatat 5998 aagacctctg gcatgaatat ttcatatcta taaaatgaca gatcccacca ggaaggaagc 6058 tgttgctttc tttgaggtga tttttttcct ttgctccctg ttgctgaaac catacagctt 6118 cataaataat tttgcttgct gaaggaagaa aaagtgtttt tcataaaccc attatccagg 6178 actgtttata gctgttggaa ggactaggtc ttccctagcc cccccagtgt gcaagggcag 6238 tgaagacttg attgtacaaa atacgttttg taaatgttgt gctgttaaca ctgcaaataa 6298 acttggtagc aaaca 6313 18 6519 DNA H. sapiens CDS (142)...(4632) 18 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca 843 Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr 220 225 230 aat act gaa cat cat caa ccc agt aat aat gat ttg aac acc act gag 891 Asn Thr Glu His His Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu 235 240 245 250 aag cgt gca gct gag agg cat cca gaa aag tat cag ggt agt tct gtt 939 Lys Arg Ala Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Ser Ser Val 255 260 265 tca aac ttg cat gtg gag cca tgt ggc aca aat act cat gcc agc tca 987 Ser Asn Leu His Val Glu Pro Cys Gly Thr Asn Thr His Ala Ser Ser 270 275 280 tta cag cat gag aac agc agt tta tta ctc act aaa gac aga atg aat 1035 Leu Gln His Glu Asn Ser Ser Leu Leu Leu Thr Lys Asp Arg Met Asn 285 290 295 gta gaa aag gct gaa ttc tgt aat aaa agc aaa cag cct ggc tta gca 1083 Val Glu Lys Ala Glu Phe Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala 300 305 310 agg agc caa cat aac aga tgg gct gga agt aag gaa aca tgt aat gat 1131 Arg Ser Gln His Asn Arg Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp 315 320 325 330 agg cgg act ccc agc aca gaa aaa aag gta gat ctg aat gct gat ccc 1179 Arg Arg Thr Pro Ser Thr Glu Lys Lys Val Asp Leu Asn Ala Asp Pro 335 340 345 ctg tgt gag aga aaa gaa tgg aat aag cag aaa ctg cca tgc tca gag 1227 Leu Cys Glu Arg Lys Glu Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu 350 355 360 aat cct aga gat act gaa gat gtt cct tgg ata aca cta aat agc agc 1275 Asn Pro Arg Asp Thr Glu Asp Val Pro Trp Ile Thr Leu Asn Ser Ser 365 370 375 att cag aaa gtt aat gag tgg ttt tcc aga agt gat gaa ctg tta ggt 1323 Ile Gln Lys Val Asn Glu Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly 380 385 390 tct gat gac tca cat gat ggg gag tct gaa tca aat gcc aaa gta gct 1371 Ser Asp Asp Ser His Asp Gly Glu Ser Glu Ser Asn Ala Lys Val Ala 395 400 405 410 gat gta ttg gac gtt cta aat gag gta gat gaa tat tct ggt tct tca 1419 Asp Val Leu Asp Val Leu Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser 415 420 425 gag aaa ata gac tta ctg gcc agt gat cct cat gag gct tta ata tgt 1467 Glu Lys Ile Asp Leu Leu Ala Ser Asp Pro His Glu Ala Leu Ile Cys 430 435 440 aaa agt gaa aga gtt cac tcc aaa tca gta gag agt aat att gaa gac 1515 Lys Ser Glu Arg Val His Ser Lys Ser Val Glu Ser Asn Ile Glu Asp 445 450 455 aaa ata ttt ggg aaa acc tat cgg aag aag gca agc ctc ccc aac tta 1563 Lys Ile Phe Gly Lys Thr Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu 460 465 470 agc cat gta act gaa aat cta att ata gga gca ttt gtt act gag cca 1611 Ser His Val Thr Glu Asn Leu Ile Ile Gly Ala Phe Val Thr Glu Pro 475 480 485 490 cag ata ata caa gag cgt ccc ctc aca aat aaa tta aag cgt aaa agg 1659 Gln Ile Ile Gln Glu Arg Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg 495 500 505 aga cct aca tca ggc ctt cat cct gag gat ttt atc aag aaa gca gat 1707 Arg Pro Thr Ser Gly Leu His Pro Glu Asp Phe Ile Lys Lys Ala Asp 510 515 520 ttg gca gtt caa aag act cct gaa atg ata aat cag gga act aac caa 1755 Leu Ala Val Gln Lys Thr Pro Glu Met Ile Asn Gln Gly Thr Asn Gln 525 530 535 acg gag cag aat ggt caa gtg atg aat att act aat agt ggt cat gag 1803 Thr Glu Gln Asn Gly Gln Val Met Asn Ile Thr Asn Ser Gly His Glu 540 545 550 aat aaa aca aaa ggt gat tct att cag aat gag aaa aat cct aac cca 1851 Asn Lys Thr Lys Gly Asp Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro 555 560 565 570 ata gaa tca ctc gaa aaa gaa tct gct ttc aaa acg aaa gct gaa cct 1899 Ile Glu Ser Leu Glu Lys Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro 575 580 585 ata agc agc agt ata agc aat atg gaa ctc gaa tta aat atc cac aat 1947 Ile Ser Ser Ser Ile Ser Asn Met Glu Leu Glu Leu Asn Ile His Asn 590 595 600 tca aaa gca cct aaa aag aat agg ctg agg agg aag tct tct acc agg 1995 Ser Lys Ala Pro Lys Lys Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg 605 610 615 cat att cat gcg ctt gaa cta gta gtc agt aga aat cta agc cca cct 2043 His Ile His Ala Leu Glu Leu Val Val Ser Arg Asn Leu Ser Pro Pro 620 625 630 aat tgt act gaa ttg caa att gat agt tgt tct agc agt gaa gag ata 2091 Asn Cys Thr Glu Leu Gln Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile 635 640 645 650 aag aaa aaa aag tac aac caa atg cca gtc agg cac agc aga aac cta 2139 Lys Lys Lys Lys Tyr Asn Gln Met Pro Val Arg His Ser Arg Asn Leu 655 660 665 caa ctc atg gaa ggt aaa gaa cct gca act gga gcc aag aag agt aac 2187 Gln Leu Met Glu Gly Lys Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn 670 675 680 aag cca aat gaa cag aca agt aaa aga cat gac agc gat act ttc cca 2235 Lys Pro Asn Glu Gln Thr Ser Lys Arg His Asp Ser Asp Thr Phe Pro 685 690 695 gag ctg aag tta aca aat gca cct ggt tct ttt act aag tgt tca aat 2283 Glu Leu Lys Leu Thr Asn Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn 700 705 710 acc agt gaa ctt aaa gaa ttt gtc aat cct agc ctt cca aga gaa gaa 2331 Thr Ser Glu Leu Lys Glu Phe Val Asn Pro Ser Leu Pro Arg Glu Glu 715 720 725 730 aaa gaa gag aaa cta gaa aca gtt aaa gtg tct aat aat gct gaa gac 2379 Lys Glu Glu Lys Leu Glu Thr Val Lys Val Ser Asn Asn Ala Glu Asp 735 740 745 ccc aaa gat ctc atg tta agt gga gaa agg gtt ttg caa act gaa aga 2427 Pro Lys Asp Leu Met Leu Ser Gly Glu Arg Val Leu Gln Thr Glu Arg 750 755 760 tct gta gag agt agc agt att tca ttg gta cct ggt act gat tat ggc 2475 Ser Val Glu Ser Ser Ser Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly 765 770 775 act cag gaa agt atc tcg tta ctg gaa gtt agc act cta ggg aag gca 2523 Thr Gln Glu Ser Ile Ser Leu Leu Glu Val Ser Thr Leu Gly Lys Ala 780 785 790 aaa aca gaa cca aat aaa tgt gtg agt cag tgt gca gca ttt gaa aac 2571 Lys Thr Glu Pro Asn Lys Cys Val Ser Gln Cys Ala Ala Phe Glu Asn 795 800 805 810 ccc aag gga cta att cat ggt tgt tcc aaa gat aat aga aat gac aca 2619 Pro Lys Gly Leu Ile His Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr 815 820 825 gaa ggc ttt aag tat cca ttg gga cat gaa gtt aac cac agt cgg gaa 2667 Glu Gly Phe Lys Tyr Pro Leu Gly His Glu Val Asn His Ser Arg Glu 830 835 840 aca agc ata gaa atg gaa gaa agt gaa ctt gat gct cag tat ttg cag 2715 Thr Ser Ile Glu Met Glu Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln 845 850 855 aat aca ttc aag gtt tca aag cgc cag tca ttt gct ccg ttt tca aat 2763 Asn Thr Phe Lys Val Ser Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn 860 865 870 cca gga aat gca gaa gag gaa tgt gca aca ttc tct gcc cac tct ggg 2811 Pro Gly Asn Ala Glu Glu Glu Cys Ala Thr Phe Ser Ala His Ser Gly 875 880 885 890 tcc tta aag aaa caa agt cca aaa gtc act ttt gaa tgt gaa caa aag 2859 Ser Leu Lys Lys Gln Ser Pro Lys Val Thr Phe Glu Cys Glu Gln Lys 895 900 905 gaa gaa aat caa gga aag aat gag tct aat atc aag cct gta cag aca 2907 Glu Glu Asn Gln Gly Lys Asn Glu Ser Asn Ile Lys Pro Val Gln Thr 910 915 920 gtt aat atc act gca ggc ttt cct gtg gtt ggt cag aaa gat aag cca 2955 Val Asn Ile Thr Ala Gly Phe Pro Val Val Gly Gln Lys Asp Lys Pro 925 930 935 gtt gat aat gcc aaa tgt agt atc aaa gga ggc tct agg ttt tgt cta 3003 Val Asp Asn Ala Lys Cys Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu 940 945 950 tca tct cag ttc aga ggc aac gaa act gga ctc att act cca aat aaa 3051 Ser Ser Gln Phe Arg Gly Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys 955 960 965 970 cat gga ctt tta caa aac cca tat cgt ata cca cca ctt ttt ccc atc 3099 His Gly Leu Leu Gln Asn Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile 975 980 985 aag tca ttt gtt aaa act aaa tgt aag aaa aat ctg cta gag gaa aac 3147 Lys Ser Phe Val Lys Thr Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn 990 995 1000 ttt gag gaa cat tca atg tca cct gaa aga gaa atg gga aat gag aac 3195 Phe Glu Glu His Ser Met Ser Pro Glu Arg Glu Met Gly Asn Glu Asn 1005 1010 1015 att cca agt aca gtg agc aca att agc cgt aat aac att aga gaa aat 3243 Ile Pro Ser Thr Val Ser Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn 1020 1025 1030 gtt ttt aaa gaa gcc agc tca agc aat att aat gaa gta ggt tcc agt 3291 Val Phe Lys Glu Ala Ser Ser Ser Asn Ile Asn Glu Val Gly Ser Ser 1035 1040 1045 1050 act aat gaa gtg ggc tcc agt att aat gaa ata ggt tcc agt gat gaa 3339 Thr Asn Glu Val Gly Ser Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu 1055 1060 1065 aac att caa gca gaa cta ggt aga aac aga ggg cca aaa ttg aat gct 3387 Asn Ile Gln Ala Glu Leu Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala 1070 1075 1080 atg ctt aga tta ggg gtt ttg caa cct gag gtc tat aaa caa agt ctt 3435 Met Leu Arg Leu Gly Val Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu 1085 1090 1095 cct gga agt aat tgt aag cat cct gaa ata aaa aag caa gaa tat gaa 3483 Pro Gly Ser Asn Cys Lys His Pro Glu Ile Lys Lys Gln Glu Tyr Glu 1100 1105 1110 gaa gta gtt cag act gtt aat aca gat ttc tct cca tat ctg att tca 3531 Glu Val Val Gln Thr Val Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser 1115 1120 1125 1130 gat aac tta gaa cag cct atg gga agt agt cat gca tct cag gtt tgt 3579 Asp Asn Leu Glu Gln Pro Met Gly Ser Ser His Ala Ser Gln Val Cys 1135 1140 1145 tct gag aca cct gat gac ctg tta gat gat ggt gaa ata aag gaa gat 3627 Ser Glu Thr Pro Asp Asp Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp 1150 1155 1160 act agt ttt gct gaa aat gac att aag gaa agt tct gct gtt ttt agc 3675 Thr Ser Phe Ala Glu Asn Asp Ile Lys Glu Ser Ser Ala Val Phe Ser 1165 1170 1175 aaa agc gtc cag aaa gga gag ctt agc agg agt cct agc cct ttc acc 3723 Lys Ser Val Gln Lys Gly Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr 1180 1185 1190 cat aca cat ttg gct cag ggt tac cga aga ggg gcc aag aaa tta gag 3771 His Thr His Leu Ala Gln Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu 1195 1200 1205 1210 tcc tca gaa gag aac tta tct agt gag gat gaa gag ctt ccc tgc ttc 3819 Ser Ser Glu Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe 1215 1220 1225 caa cac ttg tta ttt ggt aaa gta aac aat ata cct tct cag tct act 3867 Gln His Leu Leu Phe Gly Lys Val Asn Asn Ile Pro Ser Gln Ser Thr 1230 1235 1240 agg cat agc acc gtt gct acc gag tgt ctg tct aag aac aca gag gag 3915 Arg His Ser Thr Val Ala Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu 1245 1250 1255 aat tta tta tca ttg aag aat agc tta aat gac tgc agt aac cag gta 3963 Asn Leu Leu Ser Leu Lys Asn Ser Leu Asn Asp Cys Ser Asn Gln Val 1260 1265 1270 ata ttg gca aag gca tct cag gaa cat cac ctt agt gag gaa aca aaa 4011 Ile Leu Ala Lys Ala Ser Gln Glu His His Leu Ser Glu Glu Thr Lys 1275 1280 1285 1290 tgt tct gct agc ttg ttt tct tca cag tgc agt gaa ttg gaa gac ttg 4059 Cys Ser Ala Ser Leu Phe Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu 1295 1300 1305 act gca aat aca aac acc cag gat cct ttc ttg att ggt tct tcc aaa 4107 Thr Ala Asn Thr Asn Thr Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys 1310 1315 1320 caa atg agg cat cag tct gaa agc cag gga gtt ggt ctg agt gac aag 4155 Gln Met Arg His Gln Ser Glu Ser Gln Gly Val Gly Leu Ser Asp Lys 1325 1330 1335 gaa ttg gtt tca gat gat gaa gaa aga gga acg ggc ttg gaa gaa aat 4203 Glu Leu Val Ser Asp Asp Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn 1340 1345 1350 aat caa gaa gag caa agc atg gat tca aac tta ggt gaa gca gca tct 4251 Asn Gln Glu Glu Gln Ser Met Asp Ser Asn Leu Gly Glu Ala Ala Ser 1355 1360 1365 1370 ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta tcc 4299 Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu Ser 1375 1380 1385 tct cag agt gac att tta acc act cag cag agg gat acc atg caa cat 4347 Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln His 1390 1395 1400 aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg tta 4395 Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val Leu 1405 1410 1415 gaa cag cat ggg agc cag cct tct aac agc tac cct tcc atc ata agt 4443 Glu Gln His Gly Ser Gln Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser 1420 1425 1430 gac tct tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca tca 4491 Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser 1435 1440 1445 1450 gaa aaa gca gta tta act tca cag aaa agt agt gaa tac cct ata agc 4539 Glu Lys Ala Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser 1455 1460 1465 cag aat cca gaa ggc ctt tct gct gac aag ttt gag gtg tct gca gat 4587 Gln Asn Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala Asp 1470 1475 1480 agt tct acc agt aaa aat aaa gaa cca gga gtg gaa aga tgc tga 4632 Ser Ser Thr Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Cys 1485 1490 1495 gtttgtgtgt gaacggacac tgaaatattt tctaggaatt gcgggaggaa aatgggtagt 4692 tagctatttc tgggtgaccc agtctattaa agaaagaaaa atgctgaatg agcatgattt 4752 tgaagtcaga ggagatgtgg tcaatggaag aaaccaccaa ggtccaaagc gagcaagaga 4812 atcccaggac agaaagatct tcagggggct agaaatctgt tgctatgggc ccttcaccaa 4872 catgcccaca gatcaactgg aatggatggt acagctgtgt ggtgcttctg tggtgaagga 4932 gctttcatca ttcacccttg gcacaggtgt ccacccaatt gtggttgtgc agccagatgc 4992 ctggacagag gacaatggct tccatgcaat tgggcagatg tgtgaggcac ctgtggtgac 5052 ccgagagtgg gtgttggaca gtgtagcact ctaccagtgc caggagctgg acacctacct 5112 gataccccag atcccccaca gccactactg actgcagcca gccacaggta cagagccaca 5172 ggaccccaag aatgagctta caaagtggcc tttccaggcc ctgggagctc ctctcactct 5232 tcagtccttc tactgtcctg gctactaaat attttatgta catcagcctg aaaaggactt 5292 ctggctatgc aagggtccct taaagatttt ctgcttgaag tctcccttgg aaatctgcca 5352 tgagcacaaa attatggtaa tttttcacct gagaagattt taaaaccatt taaacgccac 5412 caattgagca agatgctgat tcattattta tcagccctat tctttctatt caggctgttg 5472 ttggcttagg gctggaagca cagagtggct tggcctcaag agaatagctg gtttccctaa 5532 gtttacttct ctaaaaccct gtgttcacaa aggcagagag tcagaccctt caatggaagg 5592 agagtgcttg ggatcgatta tgtgacttaa agtcagaata gtccttgggc agttctcaaa 5652 tgttggagtg gaacattggg gaggaaattc tgaggcaggt attagaaatg aaaaggaaac 5712 ttgaaacctg ggcatggtgg ctcacgcctg taatcccagc actttgggag gccaaggtgg 5772 gcagatcact ggaggtcagg agttcgaaac cagcctggcc aacatggtga aaccccatct 5832 ctactaaaaa tacagaaatt agccggtcat ggtggtggac acctgtaatc ccagctactc 5892 aggtggctaa ggcaggagaa tcacttcagc ccgggaggtg gaggttgcag tgagccaaga 5952 tcataccacg gcactccagc ctgggtgaca gtgagactgt ggctcaaaaa aaaaaaaaaa 6012 aaaggaaaat gaaactagga aaggtttctt aaagtctgag atatatttgc tagatttcta 6072 aagaatgtgt tctaaaacag cagaagattt tcaagaaccg gtttccaaag acagtcttct 6132 aattcctcat tagtaataag taaaatgttt attgttgtag ctctggtata taatccattc 6192 ctcttaaaat ataagacctc tggcatgaat atttcatatc tataaaatga cagatcccac 6252 caggaaggaa gctgttgctt tctttgaggt gatttttttc ctttgctccc tgttgctgaa 6312 accatacagc ttcataaata attttgcttg ctgaaggaag aaaaagtgtt tttcataaac 6372 ccattatcca ggactgttta tagctgttgg aaggactagg tcttccctag cccccccagt 6432 gtgcaagggc agtgaagact tgattgtaca aaatacgttt tgtaaatgtt gtgctgttaa 6492 cactgcaaat aaacttggta gcaaaca 6519 19 6986 DNA H. sapiens CDS (142)...(5610) 19 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gct gct tgt gaa 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Ala Ala Cys Glu 175 180 185 ttt tct gag acg gat gta aca aat act gaa cat cat caa ccc agt aat 747 Phe Ser Glu Thr Asp Val Thr Asn Thr Glu His His Gln Pro Ser Asn 190 195 200 aat gat ttg aac acc act gag aag cgt gca gct gag agg cat cca gaa 795 Asn Asp Leu Asn Thr Thr Glu Lys Arg Ala Ala Glu Arg His Pro Glu 205 210 215 aag tat cag ggt agt tct gtt tca aac ttg cat gtg gag cca tgt ggc 843 Lys Tyr Gln Gly Ser Ser Val Ser Asn Leu His Val Glu Pro Cys Gly 220 225 230 aca aat act cat gcc agc tca tta cag cat gag aac agc agt tta tta 891 Thr Asn Thr His Ala Ser Ser Leu Gln His Glu Asn Ser Ser Leu Leu 235 240 245 250 ctc act aaa gac aga atg aat gta gaa aag gct gaa ttc tgt aat aaa 939 Leu Thr Lys Asp Arg Met Asn Val Glu Lys Ala Glu Phe Cys Asn Lys 255 260 265 agc aaa cag cct ggc tta gca agg agc caa cat aac aga tgg gct gga 987 Ser Lys Gln Pro Gly Leu Ala Arg Ser Gln His Asn Arg Trp Ala Gly 270 275 280 agt aag gaa aca tgt aat gat agg cgg act ccc agc aca gaa aaa aag 1035 Ser Lys Glu Thr Cys Asn Asp Arg Arg Thr Pro Ser Thr Glu Lys Lys 285 290 295 gta gat ctg aat gct gat ccc ctg tgt gag aga aaa gaa tgg aat aag 1083 Val Asp Leu Asn Ala Asp Pro Leu Cys Glu Arg Lys Glu Trp Asn Lys 300 305 310 cag aaa ctg cca tgc tca gag aat cct aga gat act gaa gat gtt cct 1131 Gln Lys Leu Pro Cys Ser Glu Asn Pro Arg Asp Thr Glu Asp Val Pro 315 320 325 330 tgg ata aca cta aat agc agc att cag aaa gtt aat gag tgg ttt tcc 1179 Trp Ile Thr Leu Asn Ser Ser Ile Gln Lys Val Asn Glu Trp Phe Ser 335 340 345 aga agt gat gaa ctg tta ggt tct gat gac tca cat gat ggg gag tct 1227 Arg Ser Asp Glu Leu Leu Gly Ser Asp Asp Ser His Asp Gly Glu Ser 350 355 360 gaa tca aat gcc aaa gta gct gat gta ttg gac gtt cta aat gag gta 1275 Glu Ser Asn Ala Lys Val Ala Asp Val Leu Asp Val Leu Asn Glu Val 365 370 375 gat gaa tat tct ggt tct tca gag aaa ata gac tta ctg gcc agt gat 1323 Asp Glu Tyr Ser Gly Ser Ser Glu Lys Ile Asp Leu Leu Ala Ser Asp 380 385 390 cct cat gag gct tta ata tgt aaa agt gaa aga gtt cac tcc aaa tca 1371 Pro His Glu Ala Leu Ile Cys Lys Ser Glu Arg Val His Ser Lys Ser 395 400 405 410 gta gag agt aat att gaa gac aaa ata ttt ggg aaa acc tat cgg aag 1419 Val Glu Ser Asn Ile Glu Asp Lys Ile Phe Gly Lys Thr Tyr Arg Lys 415 420 425 aag gca agc ctc ccc aac tta agc cat gta act gaa aat cta att ata 1467 Lys Ala Ser Leu Pro Asn Leu Ser His Val Thr Glu Asn Leu Ile Ile 430 435 440 gga gca ttt gtt act gag cca cag ata ata caa gag cgt ccc ctc aca 1515 Gly Ala Phe Val Thr Glu Pro Gln Ile Ile Gln Glu Arg Pro Leu Thr 445 450 455 aat aaa tta aag cgt aaa agg aga cct aca tca ggc ctt cat cct gag 1563 Asn Lys Leu Lys Arg Lys Arg Arg Pro Thr Ser Gly Leu His Pro Glu 460 465 470 gat ttt atc aag aaa gca gat ttg gca gtt caa aag act cct gaa atg 1611 Asp Phe Ile Lys Lys Ala Asp Leu Ala Val Gln Lys Thr Pro Glu Met 475 480 485 490 ata aat cag gga act aac caa acg gag cag aat ggt caa gtg atg aat 1659 Ile Asn Gln Gly Thr Asn Gln Thr Glu Gln Asn Gly Gln Val Met Asn 495 500 505 att act aat agt ggt cat gag aat aaa aca aaa ggt gat tct att cag 1707 Ile Thr Asn Ser Gly His Glu Asn Lys Thr Lys Gly Asp Ser Ile Gln 510 515 520 aat gag aaa aat cct aac cca ata gaa tca ctc gaa aaa gaa tct gct 1755 Asn Glu Lys Asn Pro Asn Pro Ile Glu Ser Leu Glu Lys Glu Ser Ala 525 530 535 ttc aaa acg aaa gct gaa cct ata agc agc agt ata agc aat atg gaa 1803 Phe Lys Thr Lys Ala Glu Pro Ile Ser Ser Ser Ile Ser Asn Met Glu 540 545 550 ctc gaa tta aat atc cac aat tca aaa gca cct aaa aag aat agg ctg 1851 Leu Glu Leu Asn Ile His Asn Ser Lys Ala Pro Lys Lys Asn Arg Leu 555 560 565 570 agg agg aag tct tct acc agg cat att cat gcg ctt gaa cta gta gtc 1899 Arg Arg Lys Ser Ser Thr Arg His Ile His Ala Leu Glu Leu Val Val 575 580 585 agt aga aat cta agc cca cct aat tgt act gaa ttg caa att gat agt 1947 Ser Arg Asn Leu Ser Pro Pro Asn Cys Thr Glu Leu Gln Ile Asp Ser 590 595 600 tgt tct agc agt gaa gag ata aag aaa aaa aag tac aac caa atg cca 1995 Cys Ser Ser Ser Glu Glu Ile Lys Lys Lys Lys Tyr Asn Gln Met Pro 605 610 615 gtc agg cac agc aga aac cta caa ctc atg gaa ggt aaa gaa cct gca 2043 Val Arg His Ser Arg Asn Leu Gln Leu Met Glu Gly Lys Glu Pro Ala 620 625 630 act gga gcc aag aag agt aac aag cca aat gaa cag aca agt aaa aga 2091 Thr Gly Ala Lys Lys Ser Asn Lys Pro Asn Glu Gln Thr Ser Lys Arg 635 640 645 650 cat gac agc gat act ttc cca gag ctg aag tta aca aat gca cct ggt 2139 His Asp Ser Asp Thr Phe Pro Glu Leu Lys Leu Thr Asn Ala Pro Gly 655 660 665 tct ttt act aag tgt tca aat acc agt gaa ctt aaa gaa ttt gtc aat 2187 Ser Phe Thr Lys Cys Ser Asn Thr Ser Glu Leu Lys Glu Phe Val Asn 670 675 680 cct agc ctt cca aga gaa gaa aaa gaa gag aaa cta gaa aca gtt aaa 2235 Pro Ser Leu Pro Arg Glu Glu Lys Glu Glu Lys Leu Glu Thr Val Lys 685 690 695 gtg tct aat aat gct gaa gac ccc aaa gat ctc atg tta agt gga gaa 2283 Val Ser Asn Asn Ala Glu Asp Pro Lys Asp Leu Met Leu Ser Gly Glu 700 705 710 agg gtt ttg caa act gaa aga tct gta gag agt agc agt att tca ttg 2331 Arg Val Leu Gln Thr Glu Arg Ser Val Glu Ser Ser Ser Ile Ser Leu 715 720 725 730 gta cct ggt act gat tat ggc act cag gaa agt atc tcg tta ctg gaa 2379 Val Pro Gly Thr Asp Tyr Gly Thr Gln Glu Ser Ile Ser Leu Leu Glu 735 740 745 gtt agc act cta ggg aag gca aaa aca gaa cca aat aaa tgt gtg agt 2427 Val Ser Thr Leu Gly Lys Ala Lys Thr Glu Pro Asn Lys Cys Val Ser 750 755 760 cag tgt gca gca ttt gaa aac ccc aag gga cta att cat ggt tgt tcc 2475 Gln Cys Ala Ala Phe Glu Asn Pro Lys Gly Leu Ile His Gly Cys Ser 765 770 775 aaa gat aat aga aat gac aca gaa ggc ttt aag tat cca ttg gga cat 2523 Lys Asp Asn Arg Asn Asp Thr Glu Gly Phe Lys Tyr Pro Leu Gly His 780 785 790 gaa gtt aac cac agt cgg gaa aca agc ata gaa atg gaa gaa agt gaa 2571 Glu Val Asn His Ser Arg Glu Thr Ser Ile Glu Met Glu Glu Ser Glu 795 800 805 810 ctt gat gct cag tat ttg cag aat aca ttc aag gtt tca aag cgc cag 2619 Leu Asp Ala Gln Tyr Leu Gln Asn Thr Phe Lys Val Ser Lys Arg Gln 815 820 825 tca ttt gct ccg ttt tca aat cca gga aat gca gaa gag gaa tgt gca 2667 Ser Phe Ala Pro Phe Ser Asn Pro Gly Asn Ala Glu Glu Glu Cys Ala 830 835 840 aca ttc tct gcc cac tct ggg tcc tta aag aaa caa agt cca aaa gtc 2715 Thr Phe Ser Ala His Ser Gly Ser Leu Lys Lys Gln Ser Pro Lys Val 845 850 855 act ttt gaa tgt gaa caa aag gaa gaa aat caa gga aag aat gag tct 2763 Thr Phe Glu Cys Glu Gln Lys Glu Glu Asn Gln Gly Lys Asn Glu Ser 860 865 870 aat atc aag cct gta cag aca gtt aat atc act gca ggc ttt cct gtg 2811 Asn Ile Lys Pro Val Gln Thr Val Asn Ile Thr Ala Gly Phe Pro Val 875 880 885 890 gtt ggt cag aaa gat aag cca gtt gat aat gcc aaa tgt agt atc aaa 2859 Val Gly Gln Lys Asp Lys Pro Val Asp Asn Ala Lys Cys Ser Ile Lys 895 900 905 gga ggc tct agg ttt tgt cta tca tct cag ttc aga ggc aac gaa act 2907 Gly Gly Ser Arg Phe Cys Leu Ser Ser Gln Phe Arg Gly Asn Glu Thr 910 915 920 gga ctc att act cca aat aaa cat gga ctt tta caa aac cca tat cgt 2955 Gly Leu Ile Thr Pro Asn Lys His Gly Leu Leu Gln Asn Pro Tyr Arg 925 930 935 ata cca cca ctt ttt ccc atc aag tca ttt gtt aaa act aaa tgt aag 3003 Ile Pro Pro Leu Phe Pro Ile Lys Ser Phe Val Lys Thr Lys Cys Lys 940 945 950 aaa aat ctg cta gag gaa aac ttt gag gaa cat tca atg tca cct gaa 3051 Lys Asn Leu Leu Glu Glu Asn Phe Glu Glu His Ser Met Ser Pro Glu 955 960 965 970 aga gaa atg gga aat gag aac att cca agt aca gtg agc aca att agc 3099 Arg Glu Met Gly Asn Glu Asn Ile Pro Ser Thr Val Ser Thr Ile Ser 975 980 985 cgt aat aac att aga gaa aat gtt ttt aaa gaa gcc agc tca agc aat 3147 Arg Asn Asn Ile Arg Glu Asn Val Phe Lys Glu Ala Ser Ser Ser Asn 990 995 1000 att aat gaa gta ggt tcc agt act aat gaa gtg ggc tcc agt att aat 3195 Ile Asn Glu Val Gly Ser Ser Thr Asn Glu Val Gly Ser Ser Ile Asn 1005 1010 1015 gaa ata ggt tcc agt gat gaa aac att caa gca gaa cta ggt aga aac 3243 Glu Ile Gly Ser Ser Asp Glu Asn Ile Gln Ala Glu Leu Gly Arg Asn 1020 1025 1030 aga ggg cca aaa ttg aat gct atg ctt aga tta ggg gtt ttg caa cct 3291 Arg Gly Pro Lys Leu Asn Ala Met Leu Arg Leu Gly Val Leu Gln Pro 1035 1040 1045 1050 gag gtc tat aaa caa agt ctt cct gga agt aat tgt aag cat cct gaa 3339 Glu Val Tyr Lys Gln Ser Leu Pro Gly Ser Asn Cys Lys His Pro Glu 1055 1060 1065 ata aaa aag caa gaa tat gaa gaa gta gtt cag act gtt aat aca gat 3387 Ile Lys Lys Gln Glu Tyr Glu Glu Val Val Gln Thr Val Asn Thr Asp 1070 1075 1080 ttc tct cca tat ctg att tca gat aac tta gaa cag cct atg gga agt 3435 Phe Ser Pro Tyr Leu Ile Ser Asp Asn Leu Glu Gln Pro Met Gly Ser 1085 1090 1095 agt cat gca tct cag gtt tgt tct gag aca cct gat gac ctg tta gat 3483 Ser His Ala Ser Gln Val Cys Ser Glu Thr Pro Asp Asp Leu Leu Asp 1100 1105 1110 gat ggt gaa ata aag gaa gat act agt ttt gct gaa aat gac att aag 3531 Asp Gly Glu Ile Lys Glu Asp Thr Ser Phe Ala Glu Asn Asp Ile Lys 1115 1120 1125 1130 gaa agt tct gct gtt ttt agc aaa agc gtc cag aaa gga gag ctt agc 3579 Glu Ser Ser Ala Val Phe Ser Lys Ser Val Gln Lys Gly Glu Leu Ser 1135 1140 1145 agg agt cct agc cct ttc acc cat aca cat ttg gct cag ggt tac cga 3627 Arg Ser Pro Ser Pro Phe Thr His Thr His Leu Ala Gln Gly Tyr Arg 1150 1155 1160 aga ggg gcc aag aaa tta gag tcc tca gaa gag aac tta tct agt gag 3675 Arg Gly Ala Lys Lys Leu Glu Ser Ser Glu Glu Asn Leu Ser Ser Glu 1165 1170 1175 gat gaa gag ctt ccc tgc ttc caa cac ttg tta ttt ggt aaa gta aac 3723 Asp Glu Glu Leu Pro Cys Phe Gln His Leu Leu Phe Gly Lys Val Asn 1180 1185 1190 aat ata cct tct cag tct act agg cat agc acc gtt gct acc gag tgt 3771 Asn Ile Pro Ser Gln Ser Thr Arg His Ser Thr Val Ala Thr Glu Cys 1195 1200 1205 1210 ctg tct aag aac aca gag gag aat tta tta tca ttg aag aat agc tta 3819 Leu Ser Lys Asn Thr Glu Glu Asn Leu Leu Ser Leu Lys Asn Ser Leu 1215 1220 1225 aat gac tgc agt aac cag gta ata ttg gca aag gca tct cag gaa cat 3867 Asn Asp Cys Ser Asn Gln Val Ile Leu Ala Lys Ala Ser Gln Glu His 1230 1235 1240 cac ctt agt gag gaa aca aaa tgt tct gct agc ttg ttt tct tca cag 3915 His Leu Ser Glu Glu Thr Lys Cys Ser Ala Ser Leu Phe Ser Ser Gln 1245 1250 1255 tgc agt gaa ttg gaa gac ttg act gca aat aca aac acc cag gat cct 3963 Cys Ser Glu Leu Glu Asp Leu Thr Ala Asn Thr Asn Thr Gln Asp Pro 1260 1265 1270 ttc ttg att ggt tct tcc aaa caa atg agg cat cag tct gaa agc cag 4011 Phe Leu Ile Gly Ser Ser Lys Gln Met Arg His Gln Ser Glu Ser Gln 1275 1280 1285 1290 gga gtt ggt ctg agt gac aag gaa ttg gtt tca gat gat gaa gaa aga 4059 Gly Val Gly Leu Ser Asp Lys Glu Leu Val Ser Asp Asp Glu Glu Arg 1295 1300 1305 gga acg ggc ttg gaa gaa aat aat caa gaa gag caa agc atg gat tca 4107 Gly Thr Gly Leu Glu Glu Asn Asn Gln Glu Glu Gln Ser Met Asp Ser 1310 1315 1320 aac tta ggt gaa gca gca tct ggg tgt gag agt gaa aca agc gtc tct 4155 Asn Leu Gly Glu Ala Ala Ser Gly Cys Glu Ser Glu Thr Ser Val Ser 1325 1330 1335 gaa gac tgc tca ggg cta tcc tct cag agt gac att tta acc act cag 4203 Glu Asp Cys Ser Gly Leu Ser Ser Gln Ser Asp Ile Leu Thr Thr Gln 1340 1345 1350 cag agg gat acc atg caa cat aac ctg ata aag ctc cag cag gaa atg 4251 Gln Arg Asp Thr Met Gln His Asn Leu Ile Lys Leu Gln Gln Glu Met 1355 1360 1365 1370 gct gaa cta gaa gct gtg tta gaa cag cat ggg agc cag cct tct aac 4299 Ala Glu Leu Glu Ala Val Leu Glu Gln His Gly Ser Gln Pro Ser Asn 1375 1380 1385 agc tac cct tcc atc ata agt gac tct tct gcc ctt gag gac ctg cga 4347 Ser Tyr Pro Ser Ile Ile Ser Asp Ser Ser Ala Leu Glu Asp Leu Arg 1390 1395 1400 aat cca gaa caa agc aca tca gaa aaa gca gta tta act tca cag aaa 4395 Asn Pro Glu Gln Ser Thr Ser Glu Lys Ala Val Leu Thr Ser Gln Lys 1405 1410 1415 agt agt gaa tac cct ata agc cag aat cca gaa ggc ctt tct gct gac 4443 Ser Ser Glu Tyr Pro Ile Ser Gln Asn Pro Glu Gly Leu Ser Ala Asp 1420 1425 1430 aag ttt gag gtg tct gca gat agt tct acc agt aaa aat aaa gaa cca 4491 Lys Phe Glu Val Ser Ala Asp Ser Ser Thr Ser Lys Asn Lys Glu Pro 1435 1440 1445 1450 gga gtg gaa agg tca tcc cct tct aaa tgc cca tca tta gat gat agg 4539 Gly Val Glu Arg Ser Ser Pro Ser Lys Cys Pro Ser Leu Asp Asp Arg 1455 1460 1465 tgg tac atg cac agt tgc tct ggg agt ctt cag aat aga aac tac cca 4587 Trp Tyr Met His Ser Cys Ser Gly Ser Leu Gln Asn Arg Asn Tyr Pro 1470 1475 1480 tct caa gag gag ctc att aag gtt gtt gat gtg gag gag caa cag ctg 4635 Ser Gln Glu Glu Leu Ile Lys Val Val Asp Val Glu Glu Gln Gln Leu 1485 1490 1495 gaa gag tct ggg cca cac gat ttg acg gaa aca tct tac ttg cca agg 4683 Glu Glu Ser Gly Pro His Asp Leu Thr Glu Thr Ser Tyr Leu Pro Arg 1500 1505 1510 caa gat cta gag gga acc cct tac ctg gaa tct gga atc agc ctc ttc 4731 Gln Asp Leu Glu Gly Thr Pro Tyr Leu Glu Ser Gly Ile Ser Leu Phe 1515 1520 1525 1530 tct gat gac cct gaa tct gat cct tct gaa gac aga gcc cca gag tca 4779 Ser Asp Asp Pro Glu Ser Asp Pro Ser Glu Asp Arg Ala Pro Glu Ser 1535 1540 1545 gct cgt gtt ggc aac ata cca tct tca acc tct gca ttg aaa gtt ccc 4827 Ala Arg Val Gly Asn Ile Pro Ser Ser Thr Ser Ala Leu Lys Val Pro 1550 1555 1560 caa ttg aaa gtt gca gaa tct gcc cag agt cca gct gct gct cat act 4875 Gln Leu Lys Val Ala Glu Ser Ala Gln Ser Pro Ala Ala Ala His Thr 1565 1570 1575 act gat act gct ggg tat aat gca atg gaa gaa agt gtg agc agg gag 4923 Thr Asp Thr Ala Gly Tyr Asn Ala Met Glu Glu Ser Val Ser Arg Glu 1580 1585 1590 aag cca gaa ttg aca gct tca aca gaa agg gtc aac aaa aga atg tcc 4971 Lys Pro Glu Leu Thr Ala Ser Thr Glu Arg Val Asn Lys Arg Met Ser 1595 1600 1605 1610 atg gtg gtg tct ggc ctg acc cca gaa gaa ttt atg ctc gtg tac aag 5019 Met Val Val Ser Gly Leu Thr Pro Glu Glu Phe Met Leu Val Tyr Lys 1615 1620 1625 ttt gcc aga aaa cac cac atc act tta act aat cta att act gaa gag 5067 Phe Ala Arg Lys His His Ile Thr Leu Thr Asn Leu Ile Thr Glu Glu 1630 1635 1640 act act cat gtt gtt atg aaa aca gat gct gag ttt gtg tgt gaa cgg 5115 Thr Thr His Val Val Met Lys Thr Asp Ala Glu Phe Val Cys Glu Arg 1645 1650 1655 aca ctg aaa tat ttt cta gga att gcg gga gga aaa tgg gta gtt agc 5163 Thr Leu Lys Tyr Phe Leu Gly Ile Ala Gly Gly Lys Trp Val Val Ser 1660 1665 1670 tat ttc tgg gtg acc cag tct att aaa gaa aga aaa atg ctg aat gag 5211 Tyr Phe Trp Val Thr Gln Ser Ile Lys Glu Arg Lys Met Leu Asn Glu 1675 1680 1685 1690 cat gat ttt gaa gtc aga gga gat gtg gtc aat gga aga aac cac caa 5259 His Asp Phe Glu Val Arg Gly Asp Val Val Asn Gly Arg Asn His Gln 1695 1700 1705 ggt cca aag cga gca aga gaa tcc cag gac aga aag atc ttc agg ggg 5307 Gly Pro Lys Arg Ala Arg Glu Ser Gln Asp Arg Lys Ile Phe Arg Gly 1710 1715 1720 cta gaa atc tgt tgc tat ggg ccc ttc acc aac atg ccc aca gat caa 5355 Leu Glu Ile Cys Cys Tyr Gly Pro Phe Thr Asn Met Pro Thr Asp Gln 1725 1730 1735 ctg gaa tgg atg gta cag ctg tgt ggt gct tct gtg gtg aag gag ctt 5403 Leu Glu Trp Met Val Gln Leu Cys Gly Ala Ser Val Val Lys Glu Leu 1740 1745 1750 tca tca ttc acc ctt ggc aca ggt gtc cac cca att gtg gtt gtg cag 5451 Ser Ser Phe Thr Leu Gly Thr Gly Val His Pro Ile Val Val Val Gln 1755 1760 1765 1770 cca gat gcc tgg aca gag gac aat ggc ttc cat gca att ggg cag atg 5499 Pro Asp Ala Trp Thr Glu Asp Asn Gly Phe His Ala Ile Gly Gln Met 1775 1780 1785 tgt gag gca cct gtg gtg acc cga gag tgg gtg ttg gac agt gta gca 5547 Cys Glu Ala Pro Val Val Thr Arg Glu Trp Val Leu Asp Ser Val Ala 1790 1795 1800 ctc tac cag tgc cag gag ctg gac acc tac ctg ata ccc cag atc ccc 5595 Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Leu Ile Pro Gln Ile Pro 1805 1810 1815 cac agc cac tac tga ctgcagccag ccacaggtac agagccacag accccaagaa 5650 His Ser His Tyr 1820 tgagcttaca aagtggcctt tccaggccct gggagctcct ctcactcttc agtccttcta 5710 ctgtcctggc tactaaatat tttatgtaca tcagcctgaa aaggacttct ggctatgcaa 5770 gggtccctta aagattttct gcttgaagtc tcccttggaa atctgccatg agcacaaaat 5830 tatggtaatt tttcacctga gaagatttta aaaccattta aacgccacca attgagcaag 5890 atgctgattc attatttatc agccctattc tttctattca ggctgttgtt ggcttagggc 5950 tggaagcaca gagtggcttg gcctcaagag aatagctggt ttccctaagt ttacttctct 6010 aaaaccctgt gttcacaaag gcagagagtc agacccttca atggaaggag agtgcttggg 6070 atcgattatg tgacttaaag tcagaatagt ccttgggcag ttctcaaatg ttggagtgga 6130 acattgggga ggaaattctg aggcaggtat tagaaatgaa aaggaaactt gaaacctggg 6190 catggtggct cacgcctgta atcccagcac tttgggaggc caaggtgggc agatcactgg 6250 aggtcaggag ttcgaaacca gcctggccaa catggtgaaa ccccatctct actaaaaata 6310 cagaaattag ccggtcatgg tggtggacac ctgtaatccc agctactcag gtggctaagg 6370 caggagaatc acttcagccc gggaggtgga ggttgcagtg agccaagatc ataccacggc 6430 actccagcct gggtgacagt gagactgtgg ctcaaaaaaa aaaaaaaaaa aggaaaatga 6490 aactaggaaa ggtttcttaa agtctgagat atatttgcta gatttctaaa gaatgtgttc 6550 taaaacagca gaagattttc aagaaccggt ttccaaagac agtcttctaa ttcctcatta 6610 gtaataagta aaatgtttat tgttgtagct ctggtatata atccattcct cttaaaatat 6670 aagacctctg gcatgaatat ttcatatcta taaaatgaca gatcccacca ggaaggaagc 6730 tgttgctttc tttgaggtga tttttttcct ttgctccctg ttgctgaaac catacagctt 6790 cataaataat tttgcttgct gaaggaagaa aaagtgtttt tcataaaccc attatccagg 6850 actgtttata gctgttggaa ggactaggtc ttccctagcc cccccagtgt gcaagggcag 6910 tgaagacttg attgtacaaa atacgttttg taaatgttgt gctgttaaca ctgcaaataa 6970 acttggtagc aaacag 6986 20 3682 DNA H. sapiens CDS (142)...(2307) 20 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag ggt gaa gca gca tct ggg tgt gag agt gaa aca 843 Asp Ser Ala Lys Lys Gly Glu Ala Ala Ser Gly Cys Glu Ser Glu Thr 220 225 230 agc gtc tct gaa gac tgc tca ggg cta tcc tct cag agt gac att tta 891 Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Ser Gln Ser Asp Ile Leu 235 240 245 250 acc act cag cag agg gat acc atg caa cat aac ctg ata aag ctc cag 939 Thr Thr Gln Gln Arg Asp Thr Met Gln His Asn Leu Ile Lys Leu Gln 255 260 265 cag gaa atg gct gaa cta gaa gct gtg tta gaa cag cat ggg agc cag 987 Gln Glu Met Ala Glu Leu Glu Ala Val Leu Glu Gln His Gly Ser Gln 270 275 280 cct tct aac agc tac cct tcc atc ata agt gac tct tct gcc ctt gag 1035 Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser Asp Ser Ser Ala Leu Glu 285 290 295 gac ctg cga aat cca gaa caa agc aca tca gaa aaa gca gta tta act 1083 Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Glu Lys Ala Val Leu Thr 300 305 310 tca cag aaa agt agt gaa tac cct ata agc cag aat cca gaa ggc ctt 1131 Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gln Asn Pro Glu Gly Leu 315 320 325 330 tct gct gac aag ttt gag gtg tct gca gat agt tct acc agt aaa aat 1179 Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Ser Ser Thr Ser Lys Asn 335 340 345 aaa gaa cca gga gtg gaa agg tca tcc cct tct aaa tgc cca tca tta 1227 Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Ser Lys Cys Pro Ser Leu 350 355 360 gat gat agg tgg tac atg cac agt tgc tct ggg agt ctt cag aat aga 1275 Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gly Ser Leu Gln Asn Arg 365 370 375 aac tac cca tct caa gag gag ctc att aag gtt gtt gat gtg gag gag 1323 Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys Val Val Asp Val Glu Glu 380 385 390 caa cag ctg gaa gag tct ggg cca cac gat ttg acg gaa aca tct tac 1371 Gln Gln Leu Glu Glu Ser Gly Pro His Asp Leu Thr Glu Thr Ser Tyr 395 400 405 410 ttg cca agg caa gat cta gag gga acc cct tac ctg gaa tct gga atc 1419 Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Tyr Leu Glu Ser Gly Ile 415 420 425 agc ctc ttc tct gat gac cct gaa tct gat cct tct gaa gac aga gcc 1467 Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pro Ser Glu Asp Arg Ala 430 435 440 cca gag tca gct cgt gtt ggc aac ata cca tct tca acc tct gca ttg 1515 Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Ser Ser Thr Ser Ala Leu 445 450 455 aaa gtt ccc caa ttg aaa gtt gca gaa tct gcc cag agt cca gct gct 1563 Lys Val Pro Gln Leu Lys Val Ala Glu Ser Ala Gln Ser Pro Ala Ala 460 465 470 gct cat act act gat act gct ggg tat aat gca atg gaa gaa agt gtg 1611 Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Ala Met Glu Glu Ser Val 475 480 485 490 agc agg gag aag cca gaa ttg aca gct tca aca gaa agg gtc aac aaa 1659 Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Thr Glu Arg Val Asn Lys 495 500 505 aga atg tcc atg gtg gtg tct ggc ctg acc cca gaa gaa ttt atg ctc 1707 Arg Met Ser Met Val Val Ser Gly Leu Thr Pro Glu Glu Phe Met Leu 510 515 520 gtg tac aag ttt gcc aga aaa cac cac atc act tta act aat cta att 1755 Val Tyr Lys Phe Ala Arg Lys His His Ile Thr Leu Thr Asn Leu Ile 525 530 535 act gaa gag act act cat gtt gtt atg aaa aca gat gct gag ttt gtg 1803 Thr Glu Glu Thr Thr His Val Val Met Lys Thr Asp Ala Glu Phe Val 540 545 550 tgt gaa cgg aca ctg aaa tat ttt cta gga att gcg gga gga aaa tgg 1851 Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Ile Ala Gly Gly Lys Trp 555 560 565 570 gta gtt agc tat ttc tgg gtg acc cag tct att aaa gaa aga aaa atg 1899 Val Val Ser Tyr Phe Trp Val Thr Gln Ser Ile Lys Glu Arg Lys Met 575 580 585 ctg aat gag cat gat ttt gaa gtc aga gga gat gtg gtc aat gga aga 1947 Leu Asn Glu His Asp Phe Glu Val Arg Gly Asp Val Val Asn Gly Arg 590 595 600 aac cac caa ggt cca aag cga gca aga gaa tcc cag gac aga aag atc 1995 Asn His Gln Gly Pro Lys Arg Ala Arg Glu Ser Gln Asp Arg Lys Ile 605 610 615 ttc agg ggg cta gaa atc tgt tgc tat ggg ccc ttc acc aac atg ccc 2043 Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pro Phe Thr Asn Met Pro 620 625 630 aca gat caa ctg gaa tgg atg gta cag ctg tgt ggt gct tct gtg gtg 2091 Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cys Gly Ala Ser Val Val 635 640 645 650 aag gag ctt tca tca ttc acc ctt ggc aca ggt gtc cac cca att gtg 2139 Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gly Val His Pro Ile Val 655 660 665 gtt gtg cag cca gat gcc tgg aca gag gac aat ggc ttc cat gca att 2187 Val Val Gln Pro Asp Ala Trp Thr Glu Asp Asn Gly Phe His Ala Ile 670 675 680 ggg cag atg tgt gag gca cct gtg gtg acc cga gag tgg gtg ttg gac 2235 Gly Gln Met Cys Glu Ala Pro Val Val Thr Arg Glu Trp Val Leu Asp 685 690 695 agt gta gca ctc tac cag tgc cag gag ctg gac acc tac ctg ata ccc 2283 Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Leu Ile Pro 700 705 710 cag atc ccc cac agc cac tac tga ctgcagccag ccacaggtac agagccacag 2337 Gln Ile Pro His Ser His Tyr 715 720 gacccaagaa tgagcttaca aagtggcctt tccaggccct gggagctcct ctcactcttc 2397 agtccttcta ctgtcctggc tactaaatat tttatgtaca tcagcctgaa aaggacttct 2457 ggctatgcaa gggtccctta aagattttct gcttgaagtc tcccttggaa atctgccatg 2517 agcacaaaat tatggtaatt tttcacctga gaagatttta aaaccattta aacgccacca 2577 attgagcaag atgctgattc attatttatc agccctattc tttctattca ggctgttgtt 2637 ggcttagggc tggaagcaca gagtggcttg gcctcaagag aatagctggt ttccctaagt 2697 ttacttctct aaaaccctgt gttcacaaag gcagagagtc agacccttca atggaaggag 2757 agtgcttggg atcgattatg tgacttaaag tcagaatagt ccttgggcag ttctcaaatg 2817 ttggagtgga acattgggga ggaaattctg aggcaggtat tagaaatgaa aaggaaactt 2877 gaaacctggg catggtggct cacgcctgta atcccagcac tttgggaggc caaggtgggc 2937 agatcactgg aggtcaggag ttcgaaacca gcctggccaa catggtgaaa ccccatctct 2997 actaaaaata cagaaattag ccggtcatgg tggtggacac ctgtaatccc agctactcag 3057 gtggctaagg caggagaatc acttcagccc gggaggtgga ggttgcagtg agccaagatc 3117 ataccacggc actccagcct gggtgacagt gagactgtgg ctcaaaaaaa aaaaaaaaaa 3177 aggaaaatga aactaggaaa ggtttcttaa agtctgagat atatttgcta gatttctaaa 3237 gaatgtgttc taaaacagca gaagattttc aagaaccggt ttccaaagac agtcttctaa 3297 ttcctcatta gtaataagta aaatgtttat tgttgtagct ctggtatata atccattcct 3357 cttaaaatat aagacctctg gcatgaatat ttcatatcta taaaatgaca gatcccacca 3417 ggaaggaagc tgttgctttc tttgaggtga tttttttcct ttgctccctg ttgctgaaac 3477 catacagctt cataaataat tttgcttgct gaaggaagaa aaagtgtttt tcataaaccc 3537 attatccagg actgtttata gctgttggaa ggactaggtc ttccctagcc cccccagtgt 3597 gcaagggcag tgaagacttg attgtacaaa atacgttttg taaatgttgt gctgttaaca 3657 ctgcaaataa acttggtagc aaaca 3682 21 3796 DNA H. sapiens CDS (142)...(2421) 21 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aaa ttt tgc atg ctg aaa ctt ctc aac cag aag aaa ggg cct 315 Phe Cys Lys Phe Cys Met Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro 45 50 55 tca cag tgt cct tta tgt aag aat gat ata acc aaa agg agc cta caa 363 Ser Gln Cys Pro Leu Cys Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln 60 65 70 gaa agt acg aga ttt agt caa ctt gtt gaa gag cta ttg aaa atc att 411 Glu Ser Thr Arg Phe Ser Gln Leu Val Glu Glu Leu Leu Lys Ile Ile 75 80 85 90 tgt gct ttt cag ctt gac aca ggt ttg gag tat gca aac agc tat aat 459 Cys Ala Phe Gln Leu Asp Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn 95 100 105 ttt gca aaa aag gaa aat aac tct cct gaa cat cta aaa gat gaa gtt 507 Phe Ala Lys Lys Glu Asn Asn Ser Pro Glu His Leu Lys Asp Glu Val 110 115 120 tct atc atc caa agt atg ggc tac aga aac cgt gcc aaa aga ctt cta 555 Ser Ile Ile Gln Ser Met Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu 125 130 135 cag agt gaa ccc gaa aat cct tcc ttg cag gaa acc agt ctc agt gtc 603 Gln Ser Glu Pro Glu Asn Pro Ser Leu Gln Glu Thr Ser Leu Ser Val 140 145 150 caa ctc tct aac ctt gga act gtg aga act ctg agg aca aag cag cgg 651 Gln Leu Ser Asn Leu Gly Thr Val Arg Thr Leu Arg Thr Lys Gln Arg 155 160 165 170 ata caa cct caa aag acg tct gtc tac att gaa ttg gga tct gat tct 699 Ile Gln Pro Gln Lys Thr Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser 175 180 185 tct gaa gat acc gtt aat aag gca act tat tgc agt gtg gga gat caa 747 Ser Glu Asp Thr Val Asn Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln 190 195 200 gaa ttg tta caa atc acc cct caa gga acc agg gat gaa atc agt ttg 795 Glu Leu Leu Gln Ile Thr Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu 205 210 215 gat tct gca aaa aag gct gct tgt gaa ttt tct gag acg gat gta aca 843 Asp Ser Ala Lys Lys Ala Ala Cys Glu Phe Ser Glu Thr Asp Val Thr 220 225 230 aat act gaa cat cgt caa ccc agt aat aat gat ttg aac acc act gag 891 Asn Thr Glu His Arg Gln Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu 235 240 245 250 aag cgt gta gct gag agg cat cca gaa aag tat cag ggt gaa gca gca 939 Lys Arg Val Ala Glu Arg His Pro Glu Lys Tyr Gln Gly Glu Ala Ala 255 260 265 tct ggg tgt gag agt gaa aca agc gtc tct gaa gac tgc tca ggg cta 987 Ser Gly Cys Glu Ser Glu Thr Ser Val Ser Glu Asp Cys Ser Gly Leu 270 275 280 tcc tct cag agt gac att tta acc act cag cag agg gat acc atg caa 1035 Ser Ser Gln Ser Asp Ile Leu Thr Thr Gln Gln Arg Asp Thr Met Gln 285 290 295 cat aac ctg ata aag ctc cag cag gaa atg gct gaa cta gaa gct gtg 1083 His Asn Leu Ile Lys Leu Gln Gln Glu Met Ala Glu Leu Glu Ala Val 300 305 310 tta gaa cag cat ggg agc cag cct cct aac agc tac cct tcc atc ata 1131 Leu Glu Gln His Gly Ser Gln Pro Pro Asn Ser Tyr Pro Ser Ile Ile 315 320 325 330 agt gac tcc tct gcc ctt gag gac ctg cga aat cca gaa caa agc aca 1179 Ser Asp Ser Ser Ala Leu Glu Asp Leu Arg Asn Pro Glu Gln Ser Thr 335 340 345 tca gaa aaa gta tta act tca cag aaa agt agt gaa tac cct ata agc 1227 Ser Glu Lys Val Leu Thr Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser 350 355 360 cag aat cca gaa ggc ctt tct gct gac aag ttt gag gtg tct gca gat 1275 Gln Asn Pro Glu Gly Leu Ser Ala Asp Lys Phe Glu Val Ser Ala Asp 365 370 375 agt tct acc agt aaa aat aaa gaa cca gga gtg gaa agg tca tcc cct 1323 Ser Ser Thr Ser Lys Asn Lys Glu Pro Gly Val Glu Arg Ser Ser Pro 380 385 390 tct aaa tgc cca tca tta gat gat agg tgg tac atg cac agt tgc tct 1371 Ser Lys Cys Pro Ser Leu Asp Asp Arg Trp Tyr Met His Ser Cys Ser 395 400 405 410 ggg agt ctt cag aat aga aac tac cca tct caa gag gag ctc att aag 1419 Gly Ser Leu Gln Asn Arg Asn Tyr Pro Ser Gln Glu Glu Leu Ile Lys 415 420 425 gtt gtt gat gtg gag gag caa cag ctg gaa gag tct ggg cca cac gat 1467 Val Val Asp Val Glu Glu Gln Gln Leu Glu Glu Ser Gly Pro His Asp 430 435 440 ttg acg gaa aca tct tac ttg cca agg caa gat cta gag gga acc cct 1515 Leu Thr Glu Thr Ser Tyr Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro 445 450 455 tac ctg gaa tct gga atc agc ctc ttc tct gat gac cct gaa tct gat 1563 Tyr Leu Glu Ser Gly Ile Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp 460 465 470 cct tct gaa gac aga gcc cca gag tca gct cgt gtt ggc aac ata cca 1611 Pro Ser Glu Asp Arg Ala Pro Glu Ser Ala Arg Val Gly Asn Ile Pro 475 480 485 490 tct tca acc tct gca ttg aaa gtt ccc caa ttg aaa gtt gca gaa tct 1659 Ser Ser Thr Ser Ala Leu Lys Val Pro Gln Leu Lys Val Ala Glu Ser 495 500 505 gcc cag ggt cca gct gct gct cat act act gat act gct ggg tat aat 1707 Ala Gln Gly Pro Ala Ala Ala His Thr Thr Asp Thr Ala Gly Tyr Asn 510 515 520 gca atg gaa gaa agt gtg agc agg gag aag cca gaa ttg aca gct tca 1755 Ala Met Glu Glu Ser Val Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser 525 530 535 aca gaa agg gtc aac aaa aga atg tcc atg gtg gtg tct ggc ctg acc 1803 Thr Glu Arg Val Asn Lys Arg Met Ser Met Val Val Ser Gly Leu Thr 540 545 550 cca gaa gaa ttt atg ctc gtg tac aag ttt gcc aga aaa cac cac atc 1851 Pro Glu Glu Phe Met Leu Val Tyr Lys Phe Ala Arg Lys His His Ile 555 560 565 570 act tta act aat cta att act gaa gag act act cat gtt gtt atg aaa 1899 Thr Leu Thr Asn Leu Ile Thr Glu Glu Thr Thr His Val Val Met Lys 575 580 585 aca gat gct gag ttt gtg tgt gaa cgg aca ctg aaa tat ttt cta gga 1947 Thr Asp Ala Glu Phe Val Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly 590 595 600 att gcg gga gga aaa tgg gta gtt agc tat ttc tgg gtg acc cag tct 1995 Ile Ala Gly Gly Lys Trp Val Val Ser Tyr Phe Trp Val Thr Gln Ser 605 610 615 att aaa gaa aga aaa atg ctg aat gag cat gat ttt gaa gtc aga gga 2043 Ile Lys Glu Arg Lys Met Leu Asn Glu His Asp Phe Glu Val Arg Gly 620 625 630 gat gtg gtc aat gga aga aac cac caa ggt cca aag cga gca aga gaa 2091 Asp Val Val Asn Gly Arg Asn His Gln Gly Pro Lys Arg Ala Arg Glu 635 640 645 650 tcc cag gac aga aag atc ttc agg ggg cta gaa atc tgt tgc tat ggg 2139 Ser Gln Asp Arg Lys Ile Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly 655 660 665 ccc ttc acc aac atg ccc aca gat caa ctg gaa tgg atg gta cag ctg 2187 Pro Phe Thr Asn Met Pro Thr Asp Gln Leu Glu Trp Met Val Gln Leu 670 675 680 tgt ggt gct tct gtg gtg aag gag ctt tca tca ttc acc ctt ggc aca 2235 Cys Gly Ala Ser Val Val Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr 685 690 695 ggt gtc cac cca att gtg gtt gtg cag cca gat gcc tgg aca gag gac 2283 Gly Val His Pro Ile Val Val Val Gln Pro Asp Ala Trp Thr Glu Asp 700 705 710 aat ggc ttc cat gca att ggg cag atg tgt gag gca cct gtg gtg acc 2331 Asn Gly Phe His Ala Ile Gly Gln Met Cys Glu Ala Pro Val Val Thr 715 720 725 730 cga gag tgg gtg ttg gac agt gta gca ctc tac cag tgc cag gag ctg 2379 Arg Glu Trp Val Leu Asp Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu 735 740 745 gac acc tac ctg ata ccc cag atc ccc cac agc cac tac tga ctgcagccag 2431 Asp Thr Tyr Leu Ile Pro Gln Ile Pro His Ser His Tyr 750 755 ccacaggtac agagccacgg accccaagaa tgagcttaca aagtggcctt tccaggccct 2491 gggagctcct ctcactcttc agtccttcta ctgtcctggc tactaaatat tttatgtaca 2551 tcagcctgaa aaggacttct ggctatgcaa gggtccctta aagattttct gcttgaagtc 2611 tcccttggaa atctgccatg agcacaaaat tatggtaatt tttcacctga gaagatttta 2671 aaaccattta aacgccacca attgagcaag atgctgattc attatttatc agccctattc 2731 tttctattca ggctgttgtt ggcttagggc tggaagcaca gagtggcttg gcctcaagag 2791 aatagctggt ttccctaagt ttacttctct aaaaccctgt gttcacaaag gcagagagtc 2851 agacccttca atggaaggag agtgcttggg atcgattatg tgacttaaag tcagaatagt 2911 ccttgggcag ttctcaaatg ttggagtgga acattgggga ggaaattctg aggcaggtat 2971 tagaaatgaa aaggaaactt gaaacctggg catggtggct cacgcctgta atcccagcac 3031 tttgggaggc caaggtgggc agatcactgg aggtcaggag ttcgaaacca gcctggccaa 3091 catggtgaaa ccccatctct actaaaaata cagaaattag ccggtcatgg tggtggacac 3151 ctgtaatccc agctactcag gtggctaagg caggagaatc acttcagccc gggaggtgga 3211 ggttgcagtg agccaagatc ataccacggc actccagcct gggtgacagt gagactgtgg 3271 ctcaaaaaaa aaaaaaaaaa aggaaaatga aactaggaaa ggtttcttaa agtctgagat 3331 atatttgcta gatttctaaa gaatgtgttc taaaacagca gaagattttc aagaaccggt 3391 ttccaaagac agtcttctaa ttcctcatta gtaataagta aaatgtttat tgttgtagct 3451 ctggtatata atccattcct cttaaaatat aagacctctg gcatgaatat ttcatatcta 3511 taaaatgaca gatcccacca ggaaggaagc tgttgctttc tttgaggtga tttttttcct 3571 ttgctccctg ttgctgaaac catacagctt cataaataat tttgcttgct gaaggaagaa 3631 aaagtgtttt tcataaaccc attatccagg actgtttata gctgttggaa ggactaggtc 3691 ttccctagcc cccccagtgt gcaagggcag tgaagacttg attgtacaaa atacgttttg 3751 taaatgttgt gctgttaaca ctgcaaataa acttggtagc aaaca 3796 22 7224 DNA H. sapiens CDS (142)...(321) 22 aaaactgcga ctgcgcggcg tgagctcgct gagacttcct ggaccccgca ccaggctgtg 60 gggtttctca gataactggg cccctgcgct caggaggcct tcaccctctg ctctgggtaa 120 agttcattgg aacagaaaga a atg gat tta tct gct ctt cgc gtt gaa gaa 171 Met Asp Leu Ser Ala Leu Arg Val Glu Glu 1 5 10 gta caa aat gtc att aat gct atg cag aaa atc tta gag tgt ccc atc 219 Val Gln Asn Val Ile Asn Ala Met Gln Lys Ile Leu Glu Cys Pro Ile 15 20 25 tgt ctg gag ttg atc aag gaa cct gtc tcc aca aag tgt gac cac ata 267 Cys Leu Glu Leu Ile Lys Glu Pro Val Ser Thr Lys Cys Asp His Ile 30 35 40 ttt tgc aag gtc tta ctc tgt tgt ccc agc tgg agt aca gtg gtg cga 315 Phe Cys Lys Val Leu Leu Cys Cys Pro Ser Trp Ser Thr Val Val Arg 45 50 55 tca tga ggcttactgt tgccttgacc tcctaggctc aagcgatcct atcacctcag 371 Ser tctcccaagt agctgggact attttgcatg ctgaaacttc tcaaccagaa gaaagggcct 431 tcacagtgtc ctttatgtaa gaatgatata accaaaagga gcctacaaga aagtacgaga 491 tttagtcaac ttgttgaaga gctattgaaa atcatttgtg cttttcagct tgacacaggt 551 ttggagtatg caaacagcta taattttgca aaaaaggaaa ataactctcc tgaacatcta 611 aaagatgaag tttctatcat ccaaagtatg ggctacagaa accgtgccaa aagacttcta 671 cagagtgaac ccgaaaatcc ttccttgcag gaaaccagtc tcagtgtcca actctctaac 731 cttggaactg tgagaactct gaggacaaag cagcggatac aacctcaaaa gacgtctgtc 791 tacattgaat tgggatctga ttcttctgaa gataccgtta ataaggcaac ttattgcagt 851 gtgggagatc aagaattgtt acaaatcacc cctcaaggaa ccagggatga aatcagtttg 911 gattctgcaa aaaaggctgc ttgtgaattt tctgagacgg atgtaacaaa tactgaacat 971 catcaaccca gtaataatga tttgaacacc actgagaagc gtgcagctga gaggcatcca 1031 gaaaagtatc agggtagttc tgtttcaaac ttgcatgtgg agccatgtgg cacaaatact 1091 catgccagct cattacagca tgagaacagc agtttattac tcactaaaga cagaatgaat 1151 gtagaaaagg ctgaattctg taataaaagc aaacagcctg gcttagcaag gagccaacat 1211 aacagatggg ctggaagtaa ggaaacatgt aatgataggc ggactcccag cacagaaaaa 1271 aaggtagatc tgaatgctga tcccctgtgt gagagaaaag aatggaataa gcagaaactg 1331 ccatgctcag agaatcctag agatactgaa gatgttcctt ggataacact aaatagcagc 1391 attcagaaag ttaatgagtg gttttccaga agtgatgaac tgttaggttc tgatgactca 1451 catgatgggg agtctgaatc aaatgccaaa gtagctgatg tattggacgt tctaaatgag 1511 gtagatgaat attctggttc ttcagagaaa atagacttac tggccagtga tcctcatgag 1571 gctttaatat gtaaaagtga aagagttcac tccaaatcag tagagagtaa tattgaagac 1631 aaaatatttg ggaaaaccta tcggaagaag gcaagcctcc ccaacttaag ccatgtaact 1691 gaaaatctaa ttataggagc atttgttact gagccacaga taatacaaga gcgtcccctc 1751 acaaataaat taaagcgtaa aaggagacct acatcaggcc ttcatcctga ggattttatc 1811 aagaaagcag atttggcagt tcaaaagact cctgaaatga taaatcaggg aactaaccaa 1871 acggagcaga atggtcaagt gatgaatatt actaatagtg gtcatgagaa taaaacaaaa 1931 ggtgattcta ttcagaatga gaaaaatcct aacccaatag aatcactcga aaaagaatct 1991 gctttcaaaa cgaaagctga acctataagc agcagtataa gcaatatgga actcgaatta 2051 aatatccaca attcaaaagc acctaaaaag aataggctga ggaggaagtc ttctaccagg 2111 catattcatg cgcttgaact agtagtcagt agaaatctaa gcccacctaa ttgtactgaa 2171 ttgcaaattg atagttgttc tagcagtgaa gagataaaga aaaaaaagta caaccaaatg 2231 ccagtcaggc acagcagaaa cctacaactc atggaaggta aagaacctgc aactggagcc 2291 aagaagagta acaagccaaa tgaacagaca agtaaaagac atgacagcga tactttccca 2351 gagctgaagt taacaaatgc acctggttct tttactaagt gttcaaatac cagtgaactt 2411 aaagaatttg tcaatcctag ccttccaaga gaagaaaaag aagagaaact agaaacagtt 2471 aaagtgtcta ataatgctga agaccccaaa gatctcatgt taagtggaga aagggttttg 2531 caaactgaaa gatctgtaga gagtagcagt atttcattgg tacctggtac tgattatggc 2591 actcaggaaa gtatctcgtt actggaagtt agcactctag ggaaggcaaa aacagaacca 2651 aataaatgtg tgagtcagtg tgcagcattt gaaaacccca agggactaat tcatggttgt 2711 tccaaagata atagaaatga cacagaaggc tttaagtatc cattgggaca tgaagttaac 2771 cacagtcggg aaacaagcat agaaatggaa gaaagtgaac ttgatgctca gtatttgcag 2831 aatacattca aggtttcaaa gcgccagtca tttgctccgt tttcaaatcc aggaaatgca 2891 gaagaggaat gtgcaacatt ctctgcccac tctgggtcct taaagaaaca aagtccaaaa 2951 gtcacttttg aatgtgaaca aaaggaagaa aatcaaggaa agaatgagtc taatatcaag 3011 cctgtacaga cagttaatat cactgcaggc tttcctgtgg ttggtcagaa agataagcca 3071 gttgataatg ccaaatgtag tatcaaagga ggctctaggt tttgtctatc atctcagttc 3131 agaggcaacg aaactggact cattactcca aataaacatg gacttttaca aaacccatat 3191 cgtataccac cactttttcc catcaagtca tttgttaaaa ctaaatgtaa gaaaaatctg 3251 ctagaggaaa actttgagga acattcaatg tcacctgaaa gagaaatggg aaatgagaac 3311 attccaagta cagtgagcac aattagccgt aataacatta gagaaaatgt ttttaaagaa 3371 gccagctcaa gcaatattaa tgaagtaggt tccagtacta atgaagtggg ctccagtatt 3431 aatgaaatag gttccagtga tgaaaacatt caagcagaac taggtagaaa cagagggcca 3491 aaattgaatg ctatgcttag attaggggtt ttgcaacctg aggtctataa acaaagtctt 3551 cctggaagta attgtaagca tcctgaaata aaaaagcaag aatatgaaga agtagttcag 3611 actgttaata cagatttctc tccatatctg atttcagata acttagaaca gcctatggga 3671 agtagtcatg catctcaggt ttgttctgag acacctgatg acctgttaga tgatggtgaa 3731 ataaaggaag atactagttt tgctgaaaat gacattaagg aaagttctgc tgtttttagc 3791 aaaagcgtcc agaaaggaga gcttagcagg agtcctagcc ctttcaccca tacacatttg 3851 gctcagggtt accgaagagg ggccaagaaa ttagagtcct cagaagagaa cttatctagt 3911 gaggatgaag agcttccctg cttccaacac ttgttatttg gtaaagtaaa caatatacct 3971 tctcagtcta ctaggcatag caccgttgct accgagtgtc tgtctaagaa cacagaggag 4031 aatttattat cattgaagaa tagcttaaat gactgcagta accaggtaat attggcaaag 4091 gcatctcagg aacatcacct tagtgaggaa acaaaatgtt ctgctagctt gttttcttca 4151 cagtgcagtg aattggaaga cttgactgca aatacaaaca cccaggatcc tttcttgatt 4211 ggttcttcca aacaaatgag gcatcagtct gaaagccagg gagttggtct gagtgacaag 4271 gaattggttt cagatgatga agaaagagga acgggcttgg aagaaaataa tcaagaagag 4331 caaagcatgg attcaaactt aggtgaagca gcatctgggt gtgagagtga aacaagcgtc 4391 tctgaagact gctcagggct atcctctcag agtgacattt taaccactca gcagagggat 4451 accatgcaac ataacctgat aaagctccag caggaaatgg ctgaactaga agctgtgtta 4511 gaacagcatg ggagccagcc ttctaacagc tacccttcca tcataagtga ctcttctgcc 4571 cttgaggacc tgcgaaatcc agaacaaagc acatcagaaa aagcagtatt aacttcacag 4631 aaaagtagtg aataccctat aagccagaat ccagaaggcc tttctgctga caagtttgag 4691 gtgtctgcag atagttctac cagtaaaaat aaagaaccag gagtggaaag gtcatcccct 4751 tctaaatgcc catcattaga tgataggtgg tacatgcaca gttgctctgg gagtcttcag 4811 aatagaaact acccatctca agaggagctc attaaggttg ttgatgtgga ggagcaacag 4871 ctggaagagt ctgggccaca cgatttgacg gaaacatctt acttgccaag gcaagatcta 4931 gagggaaccc cttacctgga atctggaatc agcctcttct ctgatgaccc tgaatctgat 4991 ccttctgaag acagagcccc agagtcagct cgtgttggca acataccatc ttcaacctct 5051 gcattgaaag ttccccaatt gaaagttgca gaatctgccc agagtccagc tgctgctcat 5111 actactgata ctgctgggta taatgcaatg gaagaaagtg tgagcaggga gaagccagaa 5171 ttgacagctt caacagaaag ggtcaacaaa agaatgtcca tggtggtgtc tggcctgacc 5231 ccagaagaat ttatgctcgt gtacaagttt gccagaaaac accacatcac tttaactaat 5291 ctaattactg aagagactac tcatgttgtt atgaaaacag atgctgagtt tgtgtgtgaa 5351 cggacactga aatattttct aggaattgcg ggaggaaaat gggtagttag ctatttctgg 5411 gtgacccagt ctattaaaga aagaaaaatg ctgaatgagc atgattttga agtcagagga 5471 gatgtggtca atggaagaaa ccaccaaggt ccaaagcgag caagagaatc ccaggacaga 5531 aagatcttca gggggctaga aatctgttgc tatgggccct tcaccaacat gcccacagat 5591 caactggaat ggatggtaca gctgtgtggt gcttctgtgg tgaaggagct ttcatcattc 5651 acccttggca caggtgtcca cccaattgtg gttgtgcagc cagatgcctg gacagaggac 5711 aatggcttcc atgcaattgg gcagatgtgt gaggcacctg tggtgacccg agagtgggtg 5771 ttggacagtg tagcactcta ccagtgccag gagctggaca cctacctgat accccagatc 5831 ccccacagcc actactgact gcagccagcc acaggtacag agccacagga ccccaagatg 5891 agcttacaaa gtggcctttc caggccctgg gagctcctct cactcttcag tccttctact 5951 gtcctggcta ctaaatattt tatgtacatc agcctgaaaa ggacttctgg ctatgcaagg 6011 gtcccttaaa gattttctgc ttgaagtctc ccttggaaat ctgccatgag cacaaaatta 6071 tggtaatttt tcacctgaga agattttaaa accatttaaa cgccaccaat tgagcaagat 6131 gctgattcat tatttatcag ccctattctt tctattcagg ctgttgttgg cttagggctg 6191 gaagcacaga gtggcttggc ctcaagagaa tagctggttt ccctaagttt acttctctaa 6251 aaccctgtgt tcacaaaggc agagagtcag acccttcaat ggaaggagag tgcttgggat 6311 cgattatgtg acttaaagtc agaatagtcc ttgggcagtt ctcaaatgtt ggagtggaac 6371 attggggagg aaattctgag gcaggtatta gaaatgaaaa ggaaacttga aacctgggca 6431 tggtggctca cgcctgtaat cccagcactt tgggaggcca aggtgggcag atcactggag 6491 gtcaggagtt cgaaaccagc ctggccaaca tggtgaaacc ccatctctac taaaaataca 6551 gaaattagcc ggtcatggtg gtggacacct gtaatcccag ctactcaggt ggctaaggca 6611 ggagaatcac ttcagcccgg gaggtggagg ttgcagtgag ccaagatcat accacggcac 6671 tccagcctgg gtgacagtga gactgtggct caaaaaaaaa aaaaaaaaag gaaaatgaaa 6731 ctaggaaagg tttcttaaag tctgagatat atttgctaga tttctaaaga atgtgttcta 6791 aaacagcaga agattttcaa gaaccggttt ccaaagacag tcttctaatt cctcattagt 6851 aataagtaaa atgtttattg ttgtagctct ggtatataat ccattcctct taaaatataa 6911 gacctctggc atgaatattt catatctata aaatgacaga tcccaccagg aaggaagctg 6971 ttgctttctt tgaggtgatt tttttccttt gctccctgtt gctgaaacca tacagcttca 7031 taaataattt tgcttgctga aggaagaaaa agtgtttttc ataaacccat tatccaggac 7091 tgtttatagc tgttggaagg actaggtctt ccctagcccc cccagtgtgc aagggcagtg 7151 aagacttgat tgtacaaaat acgttttgta aatgttgtgc tgttaacact gcaaataaac 7211 ttggtagcaa aca 7224 23 130001 DNA H. sapiens 23 gcaggtttgt tacataggta tacacgtgtc atgttggtgt gctgcacctg ttaactcgtc 60 atttacatta aggatatctc ctaatgctat ccctcccccc tccccccacc ccacaatagg 120 ctctggtgtg tgatgttccc caccctgtgt ccaagtgtcc tcattgttca gttcccacct 180 atgagaacat gtggtgtttg gttttctgtc cttgcgatag tttgctcaga atgatggttt 240 ccagcttcat ccatgtccct acaaaggaca tgaactcatc attttttagg actgcatagt 300 atattatggt gtatatgtgc cacattttct taatccagtc tatcattgat ggacatttgg 360 gttggttcca agtctttgct attgtgaata gtgccgcaat gaacatacgt gtgcatttgt 420 ctttatagca gcatgattta taatcctttg gatatatgcc cagtaatggg atcgctgggt 480 caaatggtat ttctagttct agatccttga ggaatcacca cactgttttc cacaatggtt 540 gaactagttt acagtcccac caacggcgta aaagcgttcc tatttctcca catcctctcc 600 agcacctgtt gtttcctttt taatgactga cattctaact ggtgtgagat ggtatctcat 660 tgtggttttg atttgcatgt ctctgatggc cagtgatgat gagcattttt ccatgtgtct 720 gttggctgca taaatgtctt cttttgagaa gtgtctgctc atatcctttg cccacttttt 780 gatggggttg tttgattttt tattgtaaat ttgtttaagt tctttgtaga ttctggatat 840 tagccctttg tcagatgggt agattgtaaa aattttctcc cattctgtgg ttgcctgttc 900 actctgatgg tagtttcttt tgctgtgcag aagctcttta gtttaattag attccatttg 960 tcaattttgg cttttgttgc cactgctttt ggtgttttag tcatgaagtc tttgcccctg 1020 cctatgtcct gaatggtatt gcctaggttt tcttttaggg tttttatggt tttagatctt 1080 atgtttaagt ttttaatcca ccttgagtta atttttgtat aaggtgtaag gaaggggtcc 1140 agtttcagtt ttctgcatat ggctagccag ttttcccaat gccatttatt aaatagggaa 1200 tcctttcctc attgcctgtt tcagtctatc caatttttag atttatttct cattgtcttt 1260 gttagagacg ggcctcactt tgttgcccag gctggttttg aactcctgtt ctcaagtgac 1320 cctcccgcct tggtctccca aagtactgga attacaggcg ggagccctgc gcccggcgaa 1380 gcctgtatta agccctttta tgctcactct gcggtactgc agagagcagg gaggaagcag 1440 aggtgccctg gcatcttcag ctggaggtga gcagggtgct gagggtgtga gaggccgggc 1500 gcctggggat gggaggcggg accgcatctt caaggggacg ctgccaccct accccagagg 1560 tcagggcctc tcgcccagct ctggctctga tgtcctggag ggagggagat gctgttgcga 1620 ttcagaagat caggggaggg ccacccccat tcgagaagag tgaaaatcct gagcctgaag 1680 cagaattgga atcggttgga gccgaggctt tagagggtgg cgttgggaag agggtctggc 1740 gccgccctat ggactgttcg ggctcacgag gctgaaggct ccgaagaccg cgacctgcga 1800 accatgggaa ggttccacgc ggatgaaggc tacagccccg gccagagacc ctacactagg 1860 cctggacttc tccaccggct tatgacatga tagctcaata agctccttat ttaacgcact 1920 gttgtatcag gtccctgtcg cagccactgg ccctatagcc taataaagga gcgggtgcat 1980 gcattggatt ggtgagctac cgccacagca acgcgtccta atcaaccatc ccaaacggca 2040 gttggaagaa agttcttgca ggcctgtgct tgggcttgaa cgctgggccg gccgctgcgc 2100 tctgtggctc cctgcaggcc tgcggatcgg ccagggggct ccgatccttt tggaccgagg 2160 ctgaagcaac ggctgcacca gagaaggcct tctggctgaa ggtggaagtg cacggggtcc 2220 gcagaaccgc ctaaggcgtc ttcaggcgtg ggttacgaac tggcaggctc tcctttgtgc 2280 ttcattccat ggccagagca agacacgtgg gcaagcccaa agccaggggc tgggaaagta 2340 acctccaccc acaacgaaac catggcaagg ggtgggtgca tgtagggctg aggaattggg 2400 gccaatagtc tatctatccc gtgaggagac ctgctgtggg ggttgcacag cctgggtctg 2460 caagcttcac tgccctcggc ctgggcgtcc tgtgctcctt tggcctctct gggttaggaa 2520 agtatccctt ttatctctgc aaaggtcaga gtcccagtgt ctgctttcaa atataaaacc 2580 agctattggg ggtatgaccc tgaactgtat gagggccgcc ctttcagtaa ttctctctcc 2640 aggagtgaga acctcccttt ctcaatttta ggttagatgg gtctgagtgt gtttagtgca 2700 gttcatggtt gagcaggaag attagaaata aggacataga gacaactatt ttcttggtgt 2760 taaactcatt ttaaacaaag tggaaagtaa aggatttagt agggaaatcc tttcaccttg 2820 gcaaaagtat agtctatctg gtcacaactg ccacagcatg atccttggtg gcttggcaca 2880 agcattccct gtcctccatc aagcccataa tgtccctcag taattccact gcattttttt 2940 tgcagctgct gtgtgctgga gctgtgggga acccctcggt aatctcttgt ctgcttttta 3000 ggaactccta tctccagatc ttcttttact tcccaagcca ccccacttct ttgaaaggtc 3060 tgcaggcttg tctacctctt ctcagcttgc tctgcatgcc ttggggaagc tcttaaagca 3120 tggatcatga aggagggggg cggaggagag ggaaatgcat gtttccacaa atggaccatg 3180 agcccaccag gcaggctcta gatggggaaa aaaacccctt acattatcat gtgacttgta 3240 caagaaaaaa ggtacctgca aagggtcaag ggaccagaga ggagaacttg agaggtattc 3300 tggaggaggc gacttttgat gtgagctttc taggtgagta aagggcattg tagatgaaag 3360 gactagctgg taagtggcca gcagatagaa atacaggctg agctcagggg agggtacacc 3420 cagaggtggg gaggaaggta ggaagtgaaa aaggaggctg ggcgtggtgg ctcacgcctg 3480 taatcctagc actttgagtg tccgaggcag gcggatcact tgaggtcagg agtttgagac 3540 cagcctggcc aacatggtga aaccccatct ctactaaaac tacaaaaatt agctgggtgt 3600 ggtggtgtgc gcctgtagtc ccagctactc aggaggctaa ggtatgataa ttgcttgaac 3660 ccgggaggcg gagcttgcag tgagcgaaga tcatgccact gcactccagc ctgggtaaca 3720 gagtgagatc ctgtctcaaa aaaaaaaaaa aaggaagtga aaaaggaaag ggagaaggcc 3780 agaatggaaa ggagctaaag acagactgag caaggcagag ttggaggcca gcgcaggaag 3840 ggctcaaaac atttgcaagg acagttcaca tcccactggt atgtcagctt agatttaaag 3900 cactacccag agttattcaa agccagacag gagaactgca ggcatcagaa tgccctgggg 3960 acgggtccaa aatgcagaat cctaagcccc taaagagtca ctctacgatg agatccaaga 4020 atttgggctg gatcccactt ctcctgtccc ctgccctcac cactgaggac ctaaagcata 4080 ataaaagggg acaatctctg ccctaaataa tcccttttgg cagttacttt ctgttttcaa 4140 acttcaaatc tgtcctctgg gactaaccta ggagatgagg gataagggaa ttaacattta 4200 tggaaaatgg aggaacccac ataggcacct gtgttcacct aatattcctt accaagcagt 4260 gggtgctgcc attatctcca ttgtatggat gagaaaacag gcttaaaaga ggttaatcga 4320 ccaggtgcgg tggctcacgc ctgtaatccc agcactttgg gagaccgagg acagcggatc 4380 acgatgtcag gggatcgaga ccatcctggc taacacagtg aaaccccgtc tctactaaaa 4440 atacaaagaa aaaaaaaaat tagctgggcg tgctggtggg cgcctgtagt ccaagctact 4500 caggaagctg aggcaggaga atggcgtgaa cccgggaggc agagcttgca gtgagccaag 4560 atcgcgccac tacactccag cctgggcgac agagcgagac tccatctcaa aaaaaaaaat 4620 aaaataaaat aaagaaaaaa agaattagct gggcatggtt gcgcgcgtct gtagtcccaa 4680 gctactcggg aggctgaagc aggagaattg cttgaacccg gaggcagagg ttgcagtgag 4740 ccaagatcac gccactgcac tccagcctgg tgacagagcg agacttcgtc tctaaaaaaa 4800 gaaaaagaaa aaggaaaaaa aaaaaaagag gttaagtaac ttgggcgggg gcggccagag 4860 ccacagaact agtaagtgat agaagtagga ttctcaccta gttctttctg atgctagttg 4920 gagaggcagc tttgttcagt gggttttaga gccagggctg cttaggtttg gatctcacct 4980 ctatcccata ttatttgctg ggacttcctt aaaacagtgt ggggctcagg gcaacccaat 5040 gagtatgggg ctaagacagc tgccaccgag tcagcatttt tcacaggccc ctcgagatag 5100 cactgaagac agaaatttct aaattgaatt ttattgatgt tcaggaaaga gaagtcagtc 5160 acaacccccc ttggccctca gccccaagca gagagcccag agtgtgtgac ctcaggcaag 5220 taccaaaacc tctctgtgcc tcagttcctc atctgtaaat tggggcaaat gtcagttgat 5280 gtgaggatta aatatgatga tatcctggct gggcacaatg gctcatgcct gtaatcccat 5340 aactttggga ggctgaggcc gctggattgc ttgaggccag gagttcaaaa ccagcctggc 5400 caacatggtg aaaccccatt tctaccaaat atacaaaaat tagccaggca tggtggtgca 5460 tgcctgtagt cccagctact tgggaggctg aggcacaaga atcgcttcaa cccaggaagc 5520 agaggttgca gtgagctgag attgcgccac tgcactgcag cctggatgac agagtgagac 5580 tctgtcccaa aacaaaaaga aaagcaaagc aaagaaagaa aaggagaaaa gaaaagaaaa 5640 taaaaagctg atatcctttt tttttttttg agacggagtc tcgctctgtc accgaggctg 5700 aagtgcagtg gcacgatctc ggctcactgc aagctccgcc tcctgggttc acgccattct 5760 cctgcctcag cctcccaagt agctaggact acaggcgcct gctgccacat ttggctaatt 5820 ttttgtattt ttagtagaga cggggttcaa taaaatgaag cgaaatgggg atgaaacata 5880 atgaaccaca gcagttttct gtccctactg ttcccaccct tctggggagc aagatttcaa 5940 tggaatcttc tggtgcttct cccgacatct cttgcatgtc tcattgtttt tattattatt 6000 attattattt tgagacacaa atgagctaag cgctacttcg aattattaaa gcccatatca 6060 ctggagaaat aagatcccta ttctgaacac ctagcaataa gtaccataat atactttacc 6120 tcttcatctt cctcatccag gtattttatt ttaatactat tcagatcaaa tgaaactttt 6180 acctacaaaa gaaatacaca tttaaaggca ggttataatg tacatagaag tcaaaggatg 6240 agttgggcat atttcattac atactaaata ttttatatgg ttaaaaaaat ccacaaaatc 6300 agaagacaac aaacaaccat cacaacccac agcaaagggt taatatctgc aacacaccca 6360 gagtatcagc aaaactgcta atgatacaat taacaaccca ggaaaaagta tacataaaat 6420 tcatagaaga agtcagaaca cctaacaaat acctcagaag actttcaaac tttctggtgg 6480 tcagaacaat gcaaattgaa agcaatgaaa tgtcatctaa tcagaacagc aaattgtgtg 6540 tatgtgtgtg agcacaaaaa atgggaagac ttgggttcta gacacagctc tggcccatta 6600 ctagacataa aactgtgagc aggtcagttc acctttgagc ttcagttctt taatctgtaa 6660 aataggtcta atatgtctgt tttgccgatc tcacagtgtt accataagga tcaaattaaa 6720 aatgaatatg caagttcttt caaaatgtca ttcaaatata aaaatattat aatacaggcc 6780 aggcacagtg gctcatgtct gtaatcccag gattttggga agcagaggca ggcagatcgc 6840 ttgagtccag gagttcgaga ccagcctagc caacatggtg aaacttcgtc tctaataaaa 6900 atacaaaaat tagctgggtg tagtggcgca ggcctgtatt cccagctact caagaggctg 6960 aggcaagaga attgcttgaa tctgggaggc aaggttgcag tgcgccaaga tcatgccact 7020 gcactcccgc ctgggtgata gagcgagact ctgtctcaaa aataaaataa aaaattggcc 7080 cggtgtggtg gctcatgcct gtaatcctag caatctggga ggctgaggtg gaaggatcgt 7140 gaacctagga gttgaagacc agcctgggca acaaagccgg accctgtctc cttaaaaaaa 7200 ttaagttcaa ttaaacattt ttaaaaataa taaaccagtc attagaacca taaacctgta 7260 ctgtttttga caatgtaatg cactgccctg taaaacacta caattaagac tgttatttta 7320 aggaccctga agtctgtgaa gatcaggcac ttttttgaaa ccctaagata attatccccc 7380 agttttctcc attctttgtt tctacctaga accaagttca ccaccaaaac gcagtcctgc 7440 tgacgtcaag tattcattca tatgacatgt aattactggg gtcgttaaaa tttgggcaga 7500 atctttgtca attcaccagg accttaggca aaaaatcagg aaaatgaagt gactgactca 7560 gtctgccaaa agcggatatt ctgaaatacc actttccaac tttaagaaac acttcctgcc 7620 aggtgcggtg gctcacgcct ataatcccag cactttggga ggccgaggaa ggcagatcac 7680 gaggtcagga gatcgaggtc atcctggcta acgcggtgaa acccccatct ctactaaaaa 7740 cacaaaaaat tagctgggcg tgatggcggg tgcctgtagt cccagctact cgggaggctg 7800 aggcaagaga atggcgtgaa cccgggagac agagttcgca gtgcactagc cgcgatcgtg 7860 ccactgcact tcaggctggg cgacagagcg agactcagtc tcaaaaaaaa aagaaaaaaa 7920 agaaacacac ttccctactc gttagggaaa ttaatcttcg tctctttttc tcaaattaca 7980 caattggaaa ttaatttaga tattctggag ctcctccagc tggtgggcca actaagagaa 8040 aacaggaagt gggagattct agcttagctg gaccatatcc aggtctccat aaggaactct 8100 ctttggctgg catgtaaaaa aattctttca gcaagagcat taatcttgaa cgtgtgtaaa 8160 cacgaaagct atggttaacc ctacctgctc cttaggtcta cagccagtag agtcagatag 8220 ctgggtccta ggccttcagc tttcataatt gacattattg ttaagtccat gtgactgact 8280 caccttgtct tggcacaagt tagcttttcc tccacatcga tttttttttc tttcagcctc 8340 aacaaaatcc ctttaatgaa acaaacctgg caacccgaac tttggttact gtctccacca 8400 gaggcctgta caagccaagt tatccaagct gaggccggga gtggtggctc atgcctgtaa 8460 tcccagcact ttgggaggcc aaggcaggag gatcgcttga gctcaggagt tcaagaccag 8520 cctgggctgg tctttgagaa agcgagactt tgtctcgaaa aaaaaaaaaa aaagtgtggc 8580 ctgaaagttg agtgtttgac aaaaaggaga aacagtgcct ttccaaaacc aaaggtccct 8640 aaccaagatc tctttaacgg ggtctcgaaa aaaggagaat gggatgagaa ggatatatgg 8700 gtagtgtcat tttttaactt gcagatttca tcctagtctt ccagttatcg tttcctagca 8760 ctccatgttc ccaagatagt gtcaccaccc caaggactct ctctcatttt ctttgcctgg 8820 gccctctttc tactgaggag tcgtggcctt ccatcagtag aagccggatg ttcttgtgtc 8880 cgaaattggt gggttcttgg tctcactgac ttcaagaatg aagttgcgga ccctcacggt 8940 gagtggtaca gttcttaaag atgatgtgtc cagagtttgt tccttctgat gttcggacgt 9000 gttcagagtt acctccttct ggtggattcg tggtctcgct ggcttcagga gtgaagctgc 9060 agacctttgc ggtgagtgtt acagctctta aggcggcatg tctggagttt gttcgttcct 9120 cccgtctgga gttgttcatt cctcctggtg ggttcgtggt ctcgctggct tcaggagtga 9180 agctgcagac ctctgcggtc ggtgttacca gcagataaat gctatgcgga cccaaagagt 9240 gagcagcagc aagatttatt gcaaagagca caagaacaaa gcttccacag cgtggaagga 9300 gaccagagcg ggttgctgct gctggctcag gcagcctgca tttttttttt tttttttttt 9360 tttttttgag atggagtctc cctctgtcac ccaggctgga atgcagtggt gcaatctggg 9420 ctcactgcaa gctccgcctc ccgggttcac gccattctcc tgcctcaacc tccccagtag 9480 aggggattac aggcacccac caccgcaccc agctaatatt ttgtcttttt agtagagtcg 9540 gggtttcact gtgttagcca ggatggtctc gatctcttga cctcgtgatc cacccctcta 9600 ggcctcccaa attgctggga ttacaggtgt gagccactgg cacccagcgg ggcagcctgc 9660 ttttattccc ttatctgacc ccacccacat cctgttgatt ggtccatttt acagagagct 9720 aattggtccg ttttgacagg gtgctgattg gtgcatttac aatccctgag ctagatatac 9780 acagagtgct gattggtgca tttacaatcc tctagctaga cataaaaatt ctccaagtcc 9840 ccactacatt tgctagacac agagcactga ttggtgcgtt tacaaacctt tagctagaca 9900 cagagtgctg attggtgcat ttgcaaacct tgagctagac acagagcact gattggtgca 9960 tttacaatcc tttagctaga cacagaagtt ctccaagtgc ccaccagatt agctagatac 10020 agagtgctga ttggtgcatc cccaaacccc aagctagaca cagagtgctg actggtgcat 10080 ataaaatcct caggctagac ataaaagttt tccaagtccc catctgactc aggagcccag 10140 ctggcttcac ctagtggatc ctgcgcaggg ctgtgccggg cgcctgcact cctctcagcc 10200 cttgggcagt cgatgggacc gggcgctgag gagcaggggg cggtgcccgt cggggaggct 10260 caggccacgc tggagctcac aggggttggg agggggctcg ggcatggcgg gctgcaggtc 10320 ctgagccttg ccctgtgcag ggcggctggg gcccggtgag aattcaagcg gggtgcaggc 10380 gggccggcag tgctggggga cccggcgcac cctctgcagc tgctggcccg ggtgctaggc 10440 ccctgactgc ccggggccgg gggtgcgggg cccgctgagc ccgcgcccac ctggaactcg 10500 cgctggctgg cgagcgctgc gcgcagcccc agttcccaca cccgcctctc cctccacact 10560 tccccgcaag cagagggagc cggctctggc ttcggccagc ccagagaggg gcccccacag 10620 cgcagtggcg ggctgaaggg ctcctccagc acggccagaa tggacgccaa ggccgaggag 10680 gcgccgagag cgagcgaggg ctgctagcac gttgtcacct cgcattctga accacagact 10740 ctccaactct ccggcgcttt tcgcccactc ggtccctcag aacacgaagg gctctctcat 10800 cctgtcacta aaacgattag ctgtccggag acacggaaaa agtcgcccct cttctttgca 10860 ggattcctcc cttgaacttc tccaaaccct cttagtgtga cgtgacccca cccctagcta 10920 acccaggctg cttccttacc agcttcccgc cccctgggga ggcggcaatg caaagaccgt 10980 ccgctgccag ctctgccgct atctctgtgg ggtgaatcta acatggcgga caaagacagt 11040 aactagtccc gtttctccgc gttttcgcca agaagattgg ctcttaccac ttgtccctca 11100 aaacgaccac cccattgact ggtggcgatt gcgtcgacgg agacggggca aaagcaagct 11160 gaacccgaaa aataacaaac actggggctg aggggtggaa ctacgagtgc gcagacatgg 11220 gccagagcgc atttcccctg ccccaggcaa attcggcgct cactgcgtcc ccgcaggcca 11280 ctgaccttac aagactactt gccccagact cctggggctg gatgggaatt gtagtctccc 11340 taaagagttg tacgtatctt tttaaggcct agtttctgct ttcaaaatac gaaaacataa 11400 cactccagtc cataactgtt gacaagtaca agcgcgcaca ggtctccaat ctatccactg 11460 gatttccgtg agaattgtgc ccgctctggt attggatgtt cctctccata agactacagt 11520 ttctaaggaa cactgtggcg aagacctttc attccgcaac gcatgctgga aataattatt 11580 tccctccacc cccccaacaa tccttattac ttatatttac cgaaactgga gacctccatt 11640 agggcggaaa gagtggggga ttgggacctc ttcttacgac tgctttggac aataggtagc 11700 gattctgacc ttcgtacagc aattactgtg atgcaataag ccgcaactgg aagagtagag 11760 gctagagggc aggcacttta tggcaaactc aggtagaatt cttcctcttc cgtctctttc 11820 cttttacgtc atccgggggc agactgggtg gccaatccag agccccgaga gacgcttggc 11880 tctttctgtc cctcccatcc tctgattgta ccttgatttc gtattctgag aggctgctgc 11940 ttagcggtag ccccttggtt tccgtggcaa cggaaaagcg cgggaattac agataaatta 12000 aaactgcgac tgcgcggcgt gagctcgctg agacttcctg gacgggggac aggctgtggg 12060 gtttctcaga taactgggcc cctgcgctca ggaggccttc accctctgct ctgggtaaag 12120 gtagtagagt cccgggaaag ggacaggggg cccaagtgat gctctggggt actggcgtgg 12180 gagagtggat ttccgaagct gacagatggg tattctttga cggggggtag gggcggaacc 12240 tgagaggcgt aaggcgttgt gaaccctggg gaggggggca gtttgtaggt cgcgagggaa 12300 gcgctgagga tcaggaaggg ggcactgagt gtccgtgggg gaatcctcgt gataggaact 12360 ggaatatgcc ttgaggggga cactatgtct ttaaaaacgt cggctggtca tgaggtcagg 12420 agttccagac cagcctgacc aacgtggtga aactccgtct ctactaaaaa tacaaaaatt 12480 agccgggcgt ggtgccgctc cagctactca ggaggctgag gcaggagaat cgctagaacc 12540 cgggaggcgg aggttgcagt gagccgagat cgcgccattg cactccagcc tgggcgacag 12600 agcgagactg tctcaaaaca aaacaaaaca aaacaaaaca aaaaacaccg gctggtatgt 12660 atgagaggat gggaccttgt ggaagaagag gtgccaggaa tatgtctggg aaggggagga 12720 gacaggattt tgtgggaggg agaacttaag aactggatcc atttgcgcca ttgagaaagc 12780 gcaagaggga agtagaggag cgtcagtagt aacagatgct gccggcaggg atgtgcttga 12840 ggaggatcca gagatgagag caggtcactg ggaaaggtta ggggcgggga ggccttgatt 12900 ggtgttggtt tggtcgttgt tgattttggt tttatgcaag aaaaagaaaa caaccagaaa 12960 cattggagaa agctaaggct accaccacct acccggtcag tcactcctct gtagctttct 13020 ctttcttgga gaaaggaaaa gacccaaggg gttggcagca atatgtgaaa aaattcagaa 13080 tttatgttgt ctaattacaa aaagcaactt ctagaatctt taaaaataaa ggacgttgtc 13140 attagttctt tggtttgtat tattctaaaa ccttccaaat cttaaattta ctttatttta 13200 aaatgataaa atgaagttgt cattttataa accttttaaa aagatatata tatatgtttt 13260 tctaatgtgt taaagttcat tggaacagaa agaaatggat ttatctgctc ttcgcgttga 13320 agaagtacaa aatgtcatta atgctatgca gaaaatctta gagtgtccca tctggtaagt 13380 cagcacaaga gtgtattaat ttgggattcc tatgattatc tcctatgcaa atgaacagaa 13440 ttgaccttac atactaggga agaaaagaca tgtctagtaa gattaggcta ttgtaattgc 13500 tgatttcctt aactgaagaa ctttaaaaat atagaaaatg attccttgtt ctccatccac 13560 tctgcctctc ccactcctct ccttttcaac acaaatcctg tggtccggga aagacaggga 13620 ctctgtcttg attggttctg cactggggca ggaatctagt ttagattaac tggcattttg 13680 gcttttcttc cagctctaaa acaagctcca tcacttgaaa tggcaaaata aaatcatgga 13740 tgaggccgag ggcggtggct tatgcctgta atcccagcac tttgggaggc caaggtggta 13800 ggatcacgag gtcaggagat cgagaccatc ctggccaaca tggtgaaacc ccctctccac 13860 taaaaataca aaaattagct gggcgtagtg gcatgtgcct gtaatcccag ctactcagga 13920 ggctgaggca ggagaatcac ttgaaccagg aggcagatgt tgctgtgagc caatatggca 13980 ccactgaact ccagcgacag agctaaactc catcccaaaa aaaaaaaaaa aaaaaaaaaa 14040 acatggatga tcggtgtcgt tgagaggata ggtatttgga agaacctttg tttgaaactg 14100 gctctgtaca tacaatgaaa ttacatactt atttacatac aatgaaatgc agaggttttt 14160 tttttatata ggatctctgt cgagaggctg gagtgcagtg gtgctatcac agctcactgc 14220 agcctcaacc tcgtcaggct caagcaatcc tcccacctca gcctccagag tagcagggac 14280 gataggtgtg caccaccatg cccagctaat ttttgtattt ttttttcttt ttttgagatg 14340 gagtcttgct ctgttgccca ggctggagtg cagtggcgcg atctcagctc actgcaaact 14400 ctgcctcccg ggttcatgcc attcttctgc ctgagcctcc tgaatagctg ggactacaag 14460 cacccactac cacgcccggc taattttttg tatttttttt tcttttttag tagaggcggg 14520 atttcaccgt gttagccagg atagtcttga tctcctgacc ttgtgatcca cccgcctggg 14580 cctcccaaag tgctaggatt acaggcataa gccactgcgt ccagccattc ttgtattttt 14640 ctgttgtaga gatagggttt tgctatgttg gccatgctgg tctcaaactc ctgacctcaa 14700 gtgatctacc ctcccttggc ctctcaaggt gctgggatta caggcctgag ccattgcacc 14760 cagccatggt ctaaaaatct tgattgaaat accacctttt catttccaga cacccctatt 14820 taaaattacc acacccccag cacacacttt atcttctatt cctgctgctt ctccataaca 14880 ctgattacta gctgacattc tatgtaatgt atccattttt tatctctagt cccacagaat 14940 gtaaactcca ggatgggatt tttgttttgt ttacatacat ctgtatgttc agtagttaga 15000 acggtacttg ggacctagtt gccactcaat aaacatttgt caaataaata ataaactaaa 15060 ctaaattagt tctttaattt ttttaaatat ggtgatggtt agtagtgagt aacattcaaa 15120 aaataagttg aaaagttgta ccattgcctc ttacccacaa taaaaaaggg taaattcttt 15180 tctgctttat gaaagttgtt tttcatattt gaagtcaagt taatcagatt aaggaaaatg 15240 tatgttgtgt tttcagagcg atacaagatt tataaataac catcctctcc cttgcccttc 15300 aacattatag ctaaacaaaa ataagaggaa aacaggattc acaatttatc aatttattga 15360 aaatcagagc cagagaagca ggaaatgaca ttgtaggaaa aaactgcttt tgaaaaagca 15420 caaaacttac tcatgacaat cagtgatcag gaaaatcctc aatagtgtgg catttggata 15480 catttatgtt tcatttccat gggagagagt cataaaaata ggatgttctt tctcattctg 15540 gcaaattaaa ccatcaatta aaaactcaga tacataaaaa ttaaagatgt aagaatgaaa 15600 atgctaaatt gttattttca atcaactatt atgttttcta gcttttcatt gcttttttct 15660 gtttcctgtt aagattaatt tctttttttt tttttttttt tttttttgag acagactttg 15720 gctcttgttg cccaggctgg agtgcagtgg cacaatctcg gctcactaca acctccacct 15780 cccgggttca agcaattctg ctgcctcagc ctccggagta cctgggattg caggcatgtg 15840 ccatcacacc agctaatttt gtatttttag tagagacagg gtttctccat attggtcagg 15900 ttggtctcga actcctgacc tcaggtgatc ctcctgcctt ggcctccgaa agtgctggga 15960 ttacaggcgt gagccaccgc tcccagactt tttgttttgt tttgttttgt ttttttgaga 16020 cacggtctcg ctctgctgcc taggctggag tgcagtggca cgatcttggc tcactgccag 16080 ctccgactcc cgggttcagg ccattctcct gcctcagcct cccgagtagc tgggactaca 16140 ggcgcccacc actatgcccg gctaattttt tgtattttta gtagagacgg ggtttcacca 16200 tgttagccaa gatggtctcg atctcctgac cttgtgatcc acccgcctca gccttccaaa 16260 gtgctgggat tacagtcctg agccactgcg cccggcctgg accttttttt ttcggggtgg 16320 ggggttggag tctggctctg tcgcccaggc tggagtgcag tggcgccatc ttggctcact 16380 gcaacctccg cctgccaggt tcaagttcaa gcgcttctcc tgcctcagcc tcctgagtag 16440 ctgggattat aggcgcacgc caccgtggcc ggctaatttt gtatttttag tagagatagg 16500 gtttcatcac gttggtcagg ctggtcttga agtcctgatc tcgtgatcca cccgcctcgg 16560 ccttccaaag tgctggcgtg agccactgcg cctggcttaa gattaatttt tgtttgtttt 16620 gtttttgaga cggagtctcg ctctttcacc caggccggag tgcagtggcg ccatctcggc 16680 tcactgcaag ctccgcctcc cgggttcacg ccattctcct gcctcggccc cccaagtagc 16740 tgggactaca ggcgtccacc accacgcccg gctaattttt tgtattttta gtagagacgg 16800 ggtttcaccg tgttagccag gatggtctcc acttcctgac ctcgtgatcc gcccacctcg 16860 gcctcccaaa gtgctgggat tacaggcgtg agccaccgcg cccggcctta agattaattt 16920 ttatggtgtt ttacattcat ttgtatggaa agttctagga tagggatcat atttcacttc 16980 cttttaatat agtacagtat agcacaattt gcagttatgt cttaatatgt gatcaggaat 17040 gatcatgact ggaaacagtg ttatttgtgg tagctatagg gtaggtaagg ttttcagcct 17100 gttttaggtt tcttgaacta aaattccttc tgctgtcttc taagtcaata ttggcagcta 17160 tttctgacaa ttggtagttc tttgtaactt tttacctatg actataacat ttttgacttt 17220 cagaagaatt tgctaaaatg tgttccccgg tgggttgttg tttttcaacc taaacctagc 17280 tgctttttcc agtcacttat ccgtattgga agctcaaaat gcaaatatac agtaggccta 17340 aaatattgcc tggtttgaaa agtgtttaaa atatttgaat catttttata gtaaacattt 17400 actctcatca ggacctagaa ggggaacatt ttaatttttt ttcttttccc ttttcacagt 17460 cttccttcaa cattcattac ctttttacat atcggagttt tcatctgttc aaagtttgtg 17520 tttacagtgt gtttatatag tttagattat aattaccata ctgaaatata attgtttcag 17580 aattgagtca gtggtgagaa tgaaagccat ctggtatgat aactgaatcc aatttttctt 17640 ttacggagaa tttctttgaa atgtagctta tctcagaaat agggatttag taaccaatca 17700 gagttttctt tgtcaaggtt gtttttcttt ttaaagtcac atttggtccc agtaataata 17760 ccaatgttgg tacaagttat ctcaggttgt gaagcatttt tcccaagtca tctcaggttg 17820 tgaagcattt tcccaagtag catttaattt tattcttgca atagcccaag gagtctggca 17880 gggtgaatgg caagagaagg aaacaggttc aggtagagtg gttagcccaa ggtggctctg 17940 cttatataca caactggtag tagaaaccca gcctcctgac ttagttcatt gtttttcttt 18000 tcactgccct gtgctatgtc aaaaacccca tgattacaag agttgtatta caacccttca 18060 caataaggtt actgtccaca agcttttctt gtgatccttt tctttttttt ttttcttttt 18120 ttgagatgga ttctctgtca cccaggctgg cccgccttgg cctcccaaaa tgctgggatt 18180 acagcgtgag ccaccgcacc tggcccttgt gatccttttc taaaaagtta aatatttaag 18240 gaaaaaacca cattcttgtc acactgccag gttagtcgtt ctttgatatc ttgcctggac 18300 tttatccaaa aaatccgttt caaaaattca catttagagc taagtgtagt ggctcacgcc 18360 tgtaatcccg gtcgaggcag atggatcact tgaggtcagg acttcaagac cagcctgggc 18420 aatatggtga aaccccttcc ctaccaaaaa tacaaaaaaa ttagccgggt gtggcagcac 18480 gcgcctgtag tcccagctac ttggaatgct gaggcacaag aatcacttca atccgagagg 18540 cagaggttgc agtgagccaa gaccacacca ctgcactcca gcctgagcag cagagtgagt 18600 gagactccat ctccaaaaaa aaaaaaaaag gttcacattc agaagaaagc taaaggccgg 18660 gtatagtagc tcacacctgt aatcccagca ctttgggaag ccgaagcagg aagattgctt 18720 gatgccaggc attcaagacc agcatgggca tcatagtgag atcctgtctc tacaaaaatt 18780 aattaacatt aaaaattaaa aagatggctg gcatggtggc tcactcctgt aatcccagta 18840 ctttgggagg ccaaggcatg gtggtgcatg cctttagtcc cagctactcg ggaggctgag 18900 gcaggagaat cacttgaatt caggaggcgg aggttacaga gagccgagat ggtgccactg 18960 cactccagcc tgggcgacag aacgagactc tgtctgaaaa aaaaaaagaa aattaaaaag 19020 accagaataa agctaaagat ttaaaatagc ctataggttc ctaccagaag ttaccagcta 19080 cctctctgat agtctttccc tacaatatcc tcctggatta ttacatttta gcaccttgac 19140 ctatctgatg tcctgcatac acaggcatgg tcctgctcag ggtttgcctt ctctgctccc 19200 tctttcttgg aatgctcttc ccctaattgt tgcatagtgt gtttctttac attattaagc 19260 tatcctctag tctcacctca gtgaaacctt tcctgactcc ccccatgtac atctcacccc 19320 cacatagata ttgaactacc tgtttcccct taccctgctt aatttttctc tttaatgcac 19380 ttattcccat gtattcttta attccgtatc aactgtctac cacactagaa tatgagctct 19440 atgagagcag gctttatttt gtaaactgct acatttctat ctcctagaat agtacttgaa 19500 tatagtagta gatacttaat aaacacttgt tatattagta taataaatga actaatctca 19560 ggaatgcctt ggttttgtgg atagacaggt agggatggga acttgggtga tgtattttct 19620 gaagttttta tttttaagct tattattatt ttgagatgga gtccagctct gtcgcccagg 19680 ttggagtaca gtggcgcgat cttggctcac tgcaacgtgc acttccccgg ttcaagcgat 19740 tctcctgcct tagcctccca agtagctggg attacaggcg catgccacca tgcccagtta 19800 gttttggtat ttttagtaga gacagcgttt cactgtgttg gccaggctgg tctcgaaatc 19860 ctgacctcat gatccgcccg cctcggcctc ccaagtgctg ggattacaag catgagcccc 19920 cgtgtctggc cttattttct tttttttgag acagagtctt cctctgtcac ctaggctgga 19980 gtgcagtggc acgatattgg ctcactctgc aacctccacc tccaggattc aagtgatcct 20040 tctaccttag tctccaaagt agctgagacc acaggcatgc cccaccacgc ccggctaatt 20100 tccgtatttt aagcgtagac agggtttcac catattgtcc aggatgatct ggaactcctg 20160 agctcaggtg atccacccac ctcagcctcc caaagtgcta ggattacagg catgaggcac 20220 catgcccggc cttaagctta tcattttcta aatttccttt agtgagtact tattacactg 20280 tttttacaaa gtaatcacaa accaaacatc atgcctcttc tgaagtgatc taataagagt 20340 acacagtacc atctgtaaag tgttcttgcc agaaagttga acctgaatga ttaagcctgt 20400 aagtctagtt tataggaaat aaggctagag gaacaagtta aacctcacca tagggttata 20460 caatcagcaa aatccagaat gggggaaact ccacaggtca aatgacctaa ttttaaaaat 20520 aaatgacaag ggagaaaaag taagagacac ctatagatca gaagacactt ggggctgggc 20580 atggtggctc acacctgtaa tcccagcact ttgggaggcc aaggcaggcg gatcacctga 20640 ggtcaggagt tcaagaccag ccggccaaca tggtgaaccc caactctact aaaattacga 20700 aaaatcagcc gggcgtggtg gcgcacgcgt gtagttccaa ctacctggga ggctgaggca 20760 ggagaatcac ttgaacttgg gaggcagagg ttgcagtgag ccgagatcgc accattgcat 20820 gccagtctgg gctacaaaag caaaacccca tctcaaaaaa aagaagacac ttgggtttgg 20880 gtgtgttggc tcatgcctgt aaaccccgtg ctgggaggat tgcttgagcc caggagttca 20940 aggctgcagt gaggtatgtt tgcaccactg cactccagcc taggtgacag agtgtgacct 21000 tatcttaaaa gtaataataa ttaaaataat ctggggtagg ggtggatatg ggtgaaacag 21060 cttggccatg agttgatggt tgttggacca gggtgatggt ccatatagtt cattttatta 21120 ttttatttac ttgaaatttt gaaatacttg aaattttcca tattaagtta aaaaggcatt 21180 tacagtaaac aaaaaaaagt tctaggaagg aattcaaaag aaatataagc agaaaatttt 21240 gtctttatgg agcttaaaga tgagatgtgc acccacagtg atagtgcaga aaaatatatc 21300 actggaaatg aattcgtacg aactattatc aactaatctt ttaaatgctg atgatagtat 21360 agagtattga agggatcaat ataattctgt tttgatatct gaaagctcac tgaaggtaag 21420 gatcgtattc tctgctgtat tctcagttcc tgacacagca gacatttaat aaatattgaa 21480 cgaacttgag gccttatgtt gactcagtca taacagctca aagttgaact tattcactaa 21540 gaatagcttt atttttaaat aaattattga gcctcattta ttttcttttt ctccccccct 21600 accctgctag tctggagttg atcaaggaac ctgtctccac aaagtgtgac cacatatttt 21660 gcaagtaagt ttgaatgtgt tatgtggctc cattattagc ttttgttttt gtccttcata 21720 acccaggaaa cacctaactt tatagaagct ttactttctt caattaagtg agaacgaaaa 21780 atccaactcc atttcattct ttctcagaga gtatatagtt atcaaaagtt ggttgtaatc 21840 atagttcctg gtaaagtttt gacatatatt atcttttttt ttttttttga gacaaagtct 21900 cgctctgtcg cccaggctgg agtgcagtgg catgatcttg gctcactgca acctccgccc 21960 cccgagttca agcgattctt ctacctcagc ctcccaggta gctgggacta caggcacccg 22020 ccaccatgct tggctaattt ttgtactttt agtagagata aggtttcacc atattggcca 22080 ggctggtctc gaactcctga ccttgtgatc cacctgcctc ggcctcccaa agttctggga 22140 ttacaggcgt gagccaccac acccgactga catatattat ctattaggat gtaacatcat 22200 tttgaacagt gttttgtatt ttttgtgtcc atcagtgaaa gcaaactgca agcagttttg 22260 aaataagcac attgtgtttg agccttccca gtttctcctt tctgttcatt tctgcatatc 22320 cttatgcatt cccccttcta agggtcagtg tttgcccgct ttgtaatcat tgtgaagaca 22380 ggaaaggacc tgataccagt ttctatttag gccaaaattc atttatagca gtgattcaag 22440 ttatatttac gtatttgatg atcttgtctt ttgaaatgaa aatgtttgtt tcttaataaa 22500 agaatttcag aaaaagtaga gtaggtaatt tagtagaaca agtgggcttt ctccttttct 22560 ttatgttaag ctatggctca catcttacct taaatgtcaa ctaatttgtt tttaagtatt 22620 tatgtacctg gtacataacc tggtaccagg tacaaactat gtacttggta aaaagtttat 22680 tagcacaaaa aggtatatga tgcaaagtat acttccctct taccctacaa cccctgcctc 22740 cctgttccct ccccagacaa ccacaatgat caatttctta tgtatccttt gaggaatttt 22800 taaattccag agttcttaac ttggggttta tgaatagtct ttatgaattt cctagaatta 22860 tatttaaatt gtattcaaaa ctatggccat gtacattttt ctgggaagat agtccataat 22920 tttcatctga gtgagctaag atcatgccac tgcactccag cctgggagac aagagggaga 22980 ctcaaaaaaa aaaaagaaag gcccagtatt tactacagag agctaaagat taacctttaa 23040 agccctgggg ctttcaattt atctggatga gaatctttct ggaatgaact gtatgtttta 23100 tggtcagctt gagtaacaaa tgctgagcat actatactat tattacaggg actcaggggc 23160 ccagtgtggt agctcctgcc cataacccca gcactttggg aggccaaggc aggaggatca 23220 cttaaggcca ggagttcgaa gctgtagtga gctatgatca caccactgca ctccagccta 23280 gatgacagag tgagaccctg tctttttttt tttttgagat ggtgtttcac tctattgccc 23340 aggctggagt gcagtggtgt gatctcggct cactgcaacc tccacctcct gggttcaagc 23400 gattctcctg cctcagcctc ttgagtagct gggattacag gcatctgcca ccacacccag 23460 ctaatttttg tatttttagt cgagacaggg ttttcaccat gttggccagg ctgctctcaa 23520 actcctgact tcagctacct tggccttaaa aagtgttggg attacaggtg taagccaccg 23580 cgcctggctg accctgtctc ttaacaaaaa aagagagatt aagttatgaa tatagttgct 23640 ttgagaactt gtggaagaag gaaattatag gcttataggc agagataata atacgagcaa 23700 atgtacaaat aaaagaaaat agaggacggg cgcggtggct cacgcctata ataccagcac 23760 tttgggaggt cgaggtgggc ggatcacgag gtcaggaaat taagaccatc ctggccaaaa 23820 tggcgaaaca ctgtctctac taaaacacac aaaaaactag cctggcatgg tggcacgtac 23880 ctgtagtccc agctacttgg taggctgcgg caggggtatc acttgaacct gggaggcaga 23940 ggttgccctg agccgagatc atgccaatgc actccagcct gacaacagag tgagactctg 24000 tctgaaaaaa aagaaaagaa aagaaaatac atccaggaaa aataagctaa ctttgcatat 24060 gtgtatagga gttgtgttag aaaaggaaga agccctcaaa gatgggaagc catttgcaag 24120 aaagagaagg tccaagagga ggcagaaggg attggaaata gaaaaaggat gtaagaaaga 24180 gttgattatt actcataaac agtaatgaag gaaaaggaga gtaattctac aggaagatgc 24240 tgaggtgctt tgagcccagt gaagttggag gtaaagacag ctgttgaggc cgggcacggt 24300 ggctcacgcc tctaatccta gcacttttgg agcccaaggc aggtggatca cctgaggtca 24360 ggagctcaag accagcctga ccaacataga gaaaccccat ctctactaaa aatacaaaat 24420 tagacgggcg tggaggcgca tgcctgtaat cccagctact tgggaggctg aggcaggaga 24480 atcacttgaa cctgggaggc ggaggttgca gtgagccgag attgcgccat tgcactccag 24540 cctggccgac aagagtgaaa actgtctcaa aaaaaaaaaa caacaaaaaa cagctgttga 24600 gattgagagg attagagttg gcaactggag aagagtgaga agcttggttt caagcttgtg 24660 atagtcagga ttgtgatagt caggaaagaa ccagtcataa agatatatgt gtgtgtatac 24720 atataaatat gttatatata tgtgtgtgtg tgacacatat atatttttgt ttgtttcttt 24780 gagacagtgt ctccctctga cacccaggct ggagttcagt ggtgtgatca tagttcactt 24840 ttaccttgca atctgggttc aagcaatctc tcatctcagc ccctcaagta gctaggacta 24900 caggtacatg gcatttgccc agctaatttt taagtttctt gtagagatgg gccagccata 24960 ttttaaattg tgttttgaat gttatattag aattaaaagt ccaaagccgg gtgtggtggc 25020 tcacgcctgt aatcccagca ctttgggagg ctgaggtggg cggatcacga ggtcaggagt 25080 tcgagaccag cctggccaat atggtaacac catctctact aaaaatacaa aaattagctg 25140 ggtatggggg cacatgcctg tagtcccagc tactcaggag gctgaggcag aggaacctct 25200 tgaacccagg aggcagaggc tgcagtgagt tgagatcgtg ccactgtact ctagcctggg 25260 cgacagagca agattccgtc tcaaaaaaaa aaaaagtcca gtataatgcc catgtgatag 25320 atcgactttt tcatgaaatc tcttctgtaa tatcaatata atctgaataa cactttgatc 25380 tatatgatga gaaagctggg agcctgggag cgataccccc atgcttttgt tgtattaatt 25440 gtattttcta cggataaact ctaattgcta aaaataaaac aactttattg acccaagcaa 25500 gcctaaagtt ctgaaatctt ttttttattt ttgtttgttt gtttgtttgt ttttgtttgt 25560 tttgttttga gacggagtct cgctctgtcg cccaggctgg agtgcggtgg tgcagtctcg 25620 gctcactgca agctccacct cccgggttca caccattctc ctgcctcagc ctcccaagta 25680 gctgggacta cagacgcctg ccaccacgcc cagctaattt ttttgtattt ttagtagaga 25740 aagggtttca ccgtgttagc caggatggtc tcgatctcct gacctcgtga tctgcccgcc 25800 ttggcctccc taagttctgg gattacaagt gtgagccacc acgcccggct gttttttttt 25860 gttttgtttt gagacggagt ctcactgtgt tgcccagact ggagtgcagt ggcatgatct 25920 cagctcactg ccacctccat ctcctgggtt caagcaaatc tcctgcctca gcctcccgag 25980 tagctgggac tacaggcatg tgccaccaca cctggctaat ttttgtattt ttagtagaga 26040 cggggtttca ctatgttggc caggctggtc caaaactcct gacctcaggt gatctgctcg 26100 ccttggcctc ccacagtgcc aggattacag gcatgagcca ccttgcccag ccagttctga 26160 aatcttttat gaagcctata aaaaaagata ataataccaa tctagaaaat atttcttaag 26220 gcagtcatgc attagtttga actttccaaa caaaaaaatg caatgtgtaa tacttttttt 26280 tttttttttg agatggagtc ttgttctgtt gcccaggctg gagtgcagtg gtacaatctc 26340 ggctcactgc agcctctgcc tctctggttc aagtgattct cctgcctcag cctcccaagt 26400 agctgggatt acaggcgtgc accaccatgc atggctaatt tttgtatttt tagtagagac 26460 agggtttcac catgttgaca aggctgatct cgaactcctg acctcaggtg atccgcccac 26520 ctcagcctcc caaagtgctg agattacagg cattagccac cacgcccagc cttttatttt 26580 agtagagacc atgtttcacc atgttgacca agctggtctt gagctgacct caagtgatcc 26640 gcccacctcc acctcccaaa atggtgggat tataggcatg agccaccgca cccagcctgt 26700 aatacttttt tgaagatcta gaaccacatt gttcaaagag atagaatgtg agcaataaat 26760 gtaacttaaa tttttcaaca gctacttttt tttttttttt ttgagacagg gtcttactct 26820 gttgtcccag ctggagtaca gtggtgcgat catgaggctt actgttgcct tgacctccta 26880 ggctcaagcg atcctatcac ctcagtctcc caagtagctg ggactgtaag tgcacaccac 26940 catatccagc taaattttgt gttttctgta gagacggggt ttcgccatgt ttcccaggct 27000 ggtcttgaac tttgggctta acccgtctgc ccacctaggc atcccaaagt gctaggatta 27060 caggtgtgag tcatcatgcc tggccagtat tttagttagc tctgtctttt caagtcatat 27120 acaagttcat tttcttttaa gtttagttaa caacctttat acatgtattc tttttctagc 27180 ataaagaaag attcgaggcc gggtgcggtg gctcacgcct gtaatcccag cactttggga 27240 ggctgagatg ggcacatcac gaggtcagga gatcgagacc atcctggcta acatggtgaa 27300 accccgcctc tactaaaatt acaaaaagtt agccaggcgt ggtagcgggc acctgtagtc 27360 ccagctactc aggaggctga ggcaggagaa tggcgtgaac ccaggaggca gagcttgcag 27420 tgagcagaga ttgtgccact gcactccagc ctgagagaca gagcgagact ccgtctaaaa 27480 aaaaaaaaaa agattcgaat ccttatcttg gttgattttt gcgtatctag ttccactgaa 27540 ttatttatat aattgtatag actacagcac gagacagctt agcttgtcac tctactgtac 27600 tatattctgc agtactatca taagggaatt tcctccctac ccctgctctg aattgttcaa 27660 ttgtactatt tgctggagta atgcttgatg ccttcttgat ccattatact agagtatatg 27720 tagtatttgt agattctgaa ggagtgggag cctctattct gagttttaaa ggtacttatg 27780 tacagtggag gtagcttttt gacagcctca tcttccaaac tatagagtca ttgttttgtt 27840 gagtgcaata tggtacttga agcatctata tcggcgaaga aggacccaag tctccttgac 27900 cttacctacc tacattcact ttctctggta ggaagattgt gggtgcctct ctccagactt 27960 agtttccatg tcaaaaaaga aaaaaggaag attgtgggct ttgctacaat ccaattctgg 28020 atccaatata accttcattg cttaattact gtgtgatctg ggacaagcct ctactctata 28080 aaaatgaaga taaggccagg cttgatggct catgcctgta atcccagcac gttgggatgc 28140 caaggcagga ggatcacttg aggtcaggag ttcgagacca gactgggcaa tatagtgaaa 28200 ccacatctgt acaaaaataa agatagaaag tagcccagcg caatggctca cacctgtaat 28260 cccagcactt tgggaggctg aagcaggcga tcacttgagg tcgggagttc aagactgtag 28320 acagatagat aggtaggtag atagatagag atatagatat agttggggtt tttttgtttt 28380 gttttgtttt gtttttgaga tggagtttcg ctcttgttgc ccaggctgga gtgcaatggc 28440 gcgatctcag tttactgcaa cctccgcctc ccgggttcaa gagattctcc tgcctcagcc 28500 tcctgagtag ccaggattac aggcatatgc caccatgccc ggctaatttt tgtattttta 28560 gtagagacag ggtttctccg tgttggtcag gctggtcttg aactcctgac ctctcccaaa 28620 gtgttgggat tacaggcgtg agccaccgct cctggccttt tttttttttt tttttttttt 28680 tttgagacag agtcttcctc tgttgcccag ggtggagtgc agtggcactc ttctcagctc 28740 attgcaacct ctgccatcct gggttccagt gattctcatg cctcagcctc ccaagtagct 28800 gggactcagg cgtgtgccca ccacgcctgg ctaattttgt tgtattttta gtagagacag 28860 ggtttcacca tgttagccag gctggtctca aactccaggc ctcaagtgat ctgcctgcct 28920 cagcctcctg ggattgcaga catgagccac tgcacccggc caagagaggg taataaatgt 28980 taaattacct ggctagtaaa aaatattctc taagtgtctt ttctcacaat tcccaatgcc 29040 tttttttttt ttttggcaca atctcactct gttgcccagg ctggaatgca atggtgcaat 29100 attggctcac tgtaaccccc gcctcacagg ttcaacttat tctcatgcct cagcctcccg 29160 agtaactggg actacagtgc accaccacca cacccagcta atttttgaat atttagtaga 29220 gacagggttt caccatgttg gccaggctgg tcttgaactc ctggcctcaa gtgattcacc 29280 caccccgcaa gtgctgggat tacaggtgtg gaccaccgtg cacagcccta gtgacttttt 29340 ttttagcccc ttaatctttt ctttcctggg tctcttcatt gtcagtgtct gctatttact 29400 ccctacctag tcaccccctt caccagtata ttatgtcctt tatgttttat tttgcaggat 29460 cttattttgc ttttctattg aatcccctcc atctagaata gtactagaca tagtaaatat 29520 tggttgtatg agtgaatcgc tgcttttaat tatcatcacc attgctctct ctacttctgg 29580 tctatgatcc actttgagtt aacttttgtt atttggtgtg agataggagt ataatttcat 29640 tcttttacat gtggttatac ttttgtctca acactgtttg ttaaaaacac aaaaagtatt 29700 attttcccat ttaatcatct ttggcctggg cacggtggct catgcctgta atcccagcac 29760 tctggaaggc caaggcagat ggatcaattt gaggccagga gttcaagact agccaacatg 29820 gtgaaactaa aaatacaaaa aattagctgg gtatggtggt gcatgtctgt aatcccagct 29880 actcgggagg ctgaggcacg agaattgctt gagcctagga ggtggaggtt gtagtgagct 29940 gagattgtgt cactaccctc cagcctgggt gatagagtga gtctgtctca aaaaaaaaaa 30000 aaaaaaatta agaaaataaa aatcgtcggc caggcatggt ggctcacacc tgtaatccca 30060 gcactttggg aggcagaggc gggcagatca cgaggtcagg agatggagac catcctggct 30120 aacatggtga aaccccgtct ctactaaaaa taaaaaaatt agccgggcat ggtgctgggc 30180 gcctgtagtc ccagctgctc gggaggctga ggcaggagaa tggcgtgaac ccaggaggtg 30240 gagcttgcag tgagccgaga tcgtgccact gcactccagc ctgggagaca gagcgagact 30300 ccgtctcaaa aaaaaaaaaa aaaaaaattg tcttggtatt tattattgtt gaaaatcgct 30360 tgatcacaga tgtatgtatg agtttatttc tgtactgtca attccatttt attgatgtat 30420 gtgtctattc ttatgctatt accacacttt cttgattact atagctttgt ggtgaggtgt 30480 tgagatttta aactaattat aagcatctta catgaactac ttaccgttta tatttgatta 30540 tgcagcatga aataattatg aatatatcat taaatatgcc atattaactt ttattaagtt 30600 ttatgtgatc ataacagtaa gccatatgca tgtaagttca gttttcatag atcattgctt 30660 atgtagttta ggtttttgct tatgcagcat ccaaaaacaa ttaggaaact attgcttgta 30720 attcacctgc cattactttt taaatggctc ttaagggcag ttgtgagatt atcttttcat 30780 ggctatttgc cttttgagta ttctttctac aaaaggaagt aaattaaatt gttctttctt 30840 tctttataat ttatagattt tgcatgctga aacttctcaa ccagaagaaa gggccttcac 30900 agtgtccttt atgtaagaat gatataacca aaaggtatat aatttggtaa tgatgctagg 30960 ttggaagcaa ccacagtagg aaaaagtaga aattatttaa taacatagcg ttcctataaa 31020 accattcatc agaaaaattt ataaaagagt ttttagcaca cagtaaatta tttccaaagt 31080 tattttcctg aaagttttat gggacatctg ccttatacag gtattagaaa cttactgcct 31140 ttctctaatg cttctagtgt aaaaacttgc agacttatgt aaagtagggc tgtatcgccg 31200 tgcccccatt gtctgttaat cttgttttta tatttttgat tgtgtttcct tttctttttt 31260 tttttttttt taagacaggg tcctgctctg tcactgaggc tggagtgcag tggcgtgatc 31320 tcggctcact gtagcctctg tctcccagcc tcttcctgcc ttagcctccc aaatagctgg 31380 gactacaggc acacgctacc atgcccggcc aatttttgta ttttttgtag agatgaggtt 31440 ttaccatgtt gcccaggctg gtaactcctg agctcaggtg atctgcccac ctcggcctcc 31500 caaagtgctg gggttcacag gtgtgtgttt atttctatct aattatttac acaaacacaa 31560 tgtatttata tattgtgtat ctcttctgct acaatgtaaa ttctatgaga gtagtaattt 31620 tgtctgtctc aacactgttt ttcctaagtt tggtacatag taggcactca gatgcttaaa 31680 ggaatgaatg aattgtgctt taattccact ttactaaacc caaatctccc tttggacatt 31740 gttatctatg tgttttcaaa gaagtataat cataatttga cagaaatcct tgagaggcag 31800 aactaagtga gggattgggc agggttcaga tgttaagaac agtaagctca gcagggtgtg 31860 attgctcatg cctataaccc tagcactcta ggaggctgag gtgggatgat tgcttgaggc 31920 caggagtttg aaatcagcct gggcaacata gtgagacccc atcactacca acaaaataaa 31980 taaataaatg tacatggtgg catatgccca tagtcctagc tacttgggag gctatagtgg 32040 gaggatagct tgagtacaga agtctgaggc tgcagtgagc tatgattgtg gcactgcatg 32100 ctagcctggg caatagagca agaccctgtc tctaaattaa acaaaaaaaa aagtactcta 32160 gttttctatg caatgcatta tatctgctgt ggatttaggg cagtattata tcagataatt 32220 ttaggcattt ggtaggctta aatgaatgac aaaaagttac taaatcactg ccatcacacg 32280 gtttatacag atgtcaatga tgtattgatt atagaggttt tctactgttg ctgcatctta 32340 tttttatttg tttacatgtc ttttcttatt ttagtgtcct taaaaggttg ataatcactt 32400 gctgagtgtg tttctcaaac aatttaattt caggagccta caagaaagta cgagatttag 32460 tcaacttgtt gaagagctat tgaaaatcat ttgtgctttt cagcttgaca caggtttgga 32520 gtgtaagtgt tgaatatccc aagaatgcaa ctcaagtgct gtccatgaaa actcaggaag 32580 tttgcacaat tactttctat gacgtggtga taagaccttt tagtctaggt taattttagt 32640 tctgtatctg taatctattt ttaaaaaatt actcccactg gtctcacacc ttattttatc 32700 aatcgtaagg tgcacatttt tcacatctta acatctctga aattgggaac attttactat 32760 tgagggtgtg tcatttgttt aatttgtgtg ctttctttct tagtgataca cgaaataata 32820 gtgccactta cattgttggt gtcttagctt tagtgaaata cagtattgat aggcaaattt 32880 cttagtgtta aggtagaaaa caaggactct aaataacttt gatggtctgt gtatttgttt 32940 ttgtttccta ggagtaaaat ttccagttga ttttttaaaa tttgattttt aaaaaaaatc 33000 acaggtaacc ttaatgcatt gtcttaacac aacaaagagc atacataggg tttctcttgg 33060 tttctttgat tataattcat acatttttct ctaactgcaa acataatgtt ttcccttgta 33120 ttttacagat gcaaacagct ataattttgc aaaaaaggaa aataactctc ctgaacatct 33180 aaaagatgaa gtttctatca tccaaagtat gggctacaga aaccgtgcca aaagacttct 33240 acagagtgaa cccgaaaatc cttccttggt aaaaccattt gttttcttct tcttcttctt 33300 cttcttttct tttttttttc tttttttttt ttgagatgga gtcttgctct gtggcccagg 33360 ctagaagcag tcctcctgcc ttagccccct tagtagctgg gattacaggc acgcgccacc 33420 atgccaggct aatttttgta tttttagtag agacggggtt tcatcatgtt ggccaggctg 33480 gtctcgaact cctaacctca ggtgatccac ccacctcggc tccccaaatt gctgggatta 33540 caggtgtgag ccactgtgcc cggccggtaa aaccattttc atttattctg gcaacatctc 33600 tttattgagc attgtgaata tgttagtgaa tgtgctagat gctcatagat ttatataaaa 33660 agttagtgaa gaaggaaaga tggtatatta agtggttaga caagtgttct aatcagttag 33720 agttcagaga aggtcagggt acctgatata atcaagagag agaccttaca gccaggtgag 33780 gtgaatgtac ctataatccc agctacttag gaggctgaaa tgggaggatc acttgagtcc 33840 aggtttgaga ccagcccagg caacatagca agatccccat cagatacacc aaaaagacag 33900 atttcttttt tttttttttt tttgagacag agtctcgctc tgtcgcccag gctggagcgc 33960 agtgacacga tgtcagctca ctgcaacctc cgcctcccag gttcaagtga ttctcctgcc 34020 tcagcctcct gagtagttgg gactacaggg gtacgacacc agacctggct aatttttgta 34080 attttagtag agtcggggtt tcaccatatt ggtcaggctg gtctcgaact cctgacctca 34140 ggtgatccac cctccttggc ctcccagagt gctgggatta caggcgtgag ccaccaagcc 34200 cggccaaaaa agagagctct tataggccct tccttgcttt ggagctttat ctgctctgtg 34260 atgcttatct aaaatagcca taaggtcact gatattttta agcatttgga aattacttca 34320 gctgggtgcc atggctcatg cctataatcc caaccctttg ggaggctgag gtaggaggtc 34380 ctttgagccc agcttgggca acacagtgag acactgtctc tgcaattaaa aaaaaaaaaa 34440 aagtagctgg gtgccgtggc tcacgcctgt aattccagca ctaggaggct tgaggattgc 34500 ctgagctcag gagttcaaga ccagtttggg caacatagca agtccttgtc tatattaaaa 34560 gtttttttaa attatctggg catggtggtg tgtgcctgta gtcccagcta cttgggaagc 34620 tgagacagaa ggatcacttg agtccaggag atgtagacta cagtgagcta tgatcactcc 34680 actgcacttc agcgtgggcg gcaaagcaag atctagttgc aaaaaaaaaa agaactggct 34740 gggtgcggcg gctaacacct gcaatcccag caccttggga ggctgaggcc agtggatcat 34800 gaggtcagga gattgagacc accctggcca acatggtgaa acccggtctc tactaaaaat 34860 acaaaaatta gctgggtgtg gtggcacgtg cctgtaatcc cagctactcc agaggctgag 34920 gatggagaat cacttgaacc tgagagtcgg aggttgcagt gagccgagat tgcgccactg 34980 cactccagcc tggcgacaga gcgagactcc gtctcaaaaa aaaaaaaaaa aaagcttcac 35040 gcctgtaatc ccagcacttt gggaggccga gtcaagtgga tcacgaggtg tggagatcaa 35100 gactatcctg gctcacatgg tgaaagcccg tctctactaa aaacacagaa aaattagctg 35160 agcgtgatgg cggactcctg tagtcccagc tactcgggag gctgaggcag gagaatagca 35220 tgaacccggg aggtggagct tgcagtgagc cgagatcccg ccactgcgat ccagcctggg 35280 cgacagagtg agactctgtc tcaaaaaaaa aacaaaaaaa cttagctggg cgtggtggta 35340 tgcacctgtg gtcctagcta cttgggaggc tgaggctgga gcattgcttt aacatagaga 35400 gtcaaggctg cagttgagct atgactgtgc cactggactc cagcgcaggt gactgagacc 35460 ctatctttta aaaaaaggga aaattacttg aacttaaaag gtgtaattgt taaagaaaat 35520 gtagtgattt gctctgttgt tacttatatg tgcatgaatg atggagatct taaaaagtaa 35580 tcattctggg gctgggcgta gtagcttgca cctgtaatcc cagcacttcg ggaggctgag 35640 gcaggcagat aatttgaggt caggagtttg agaccagcct ggccaacatg gtgaaaccca 35700 tctctactaa aaatacaaaa attagctggg tgtggtggca cgtacctgta atcccagcta 35760 ctcgggaggc ggaggcacaa gaattgcttg aacctaggac gcggaggttg cagcgagcca 35820 agatcgcgcc actgcactcc agcctgggcc gtagagtgag actctgtctc aaaaaagaaa 35880 aaaaagtaat tgttctagct gggcgcagtg gctcttgcct gtaatcccag cactttggga 35940 ggccaaggcg ggtggatctc gagtcctaga gttcaagacc agcctaggca atgtggtgaa 36000 accccatcgc tacaaaaaat acaaaaatta gccaggcatg gtggcgtgcg catgtagtcc 36060 cagctccttg ggaggctgag gtgggaggat cacttgaacc caggagacag aggttgcagt 36120 gaaccgagat cacgccacca cgctccagcc tgggcaacag aacaagactc tgtctaaaaa 36180 aatacaaata aaataaaagt agttctcaca gtaccagcat tcatttttca aaagatatag 36240 agctaaaaag gaaggaaaaa aaaagtaatg ttgggctttt aaatactcgt tcctatacta 36300 aatgttctta ggagtgctgg ggttttattg tcatcattta tcctttttaa aaatgttatt 36360 ggccaggcac ggtggctcat ggctgtaatc ccagcacttt gggaggccga ggcaggcaga 36420 tcacctgagg tcaggagtgt gagaccagcc tggccaacat ggcgaaacct gtctctacta 36480 aaaatacaaa aattaactag gcgtggtggt gtacgcctgt agtcccagct actcgggagg 36540 ctgaggcagg agaatcaact gaaccaggga ggtggaggtt gcagtgtgcc gagatcacgc 36600 cactgcactc tagcctggca acagagcaag attctgtctc aaaaaaaaaa aacatatata 36660 cacatatatc ccaaagtgct gggattacat atatatatat atatatatat catatctata 36720 tatatatata tgtaatatat atgttatata tatattacat atatatatgt tatatatatg 36780 ttatatatat ataatatata tatgttatat atatgttata tatatatata cacacacaca 36840 cacatatata tgtatatata tatacacaca cacacacata ttagccaggc atagttgcac 36900 acgcttgtag acccagctac tcaggaggct gaggcaggag aatctcttga acttaggagg 36960 cggaggttgc agtgagctga gattgcgcca ctgcactcca gcctgggtga cagagcagga 37020 ctctgtacac cccccaaaac aaaaaaaaaa gttatcagat gtgattggaa tgtatatcaa 37080 gtatcagctt caaaatatgc tatattaata cttcaaaaat tacacaaata atacataatc 37140 aggtttgaaa aatttaagac aacagaaaaa aaaattcaaa tcacacatat cccacacatt 37200 ttattattac tactactatt attttgtaga gactgggtct cactctgttg cttatgctgg 37260 tcttgaactc ctggcctcaa gcagtcctgc tccagcctcc caaagtgctg ggattatagg 37320 catgagctac cgctcccagc cccagacatt ttagtgtgta aattcctggg cattttttcc 37380 aggcatcata catgttagct gactgatgat ggtcaattta ttttgtccat ggtgtcaagt 37440 ttctcttcag gaggaaaagc acagaactgg ccaataattg cttgactgtt ctttaccata 37500 ctgtttagca ggaaaccagt ctcagtgtcc aactctctaa ccttggaact gtgagaactc 37560 tgaggacaaa gcagcggata caacctcaaa agacgtctgt ctacattgaa ttgggtaagg 37620 gtctcaggtt ttttaagtat ttaataataa ttgctggatt ccttatctta tagttttgcc 37680 aaaaatcttg gtcataattt gtatttgtgg taggcagctt tgggaagtga attttatgag 37740 ccctatggtg agttataaaa aatgtaaaag acgcagttcc caccttgaag aatcttactt 37800 taaaaaggga gcaaaagagg ccaggcatgg tggctcacac ctgtaatccc agcactttgg 37860 gaggccaaag tgggtggatc acctgaggtc gggagttcga gaccagccta gccaacatgg 37920 agaaactctg tctgtaccaa aaaataaaaa attagccagg tgtggtggca cataactgta 37980 atcccagcta ctcgggaggc tgaggcagga gaatcacttg aacccgggag gtggaggttg 38040 cggtgaaccg agatcgcacc attgcactcc agcctgggca aaaatagcga aactccatct 38100 aaaaaaaaaa aagagagcaa aagaaagaat atctggtttt aaatatgtgt aaatatgttt 38160 tggaaagatg gagagtagca ataaggaaaa acatgatgga ttgctacagt atttagttcc 38220 aagataaatt gtactagatg aggaagcctt ttaagaagag ctgaattgcc aggcgcagtg 38280 ctcacgcctg taatcccagc actttggaag gccgaggtgg gcggatcacc tgaggtcggg 38340 agttcaagac cagcctgacc aacatggaga aaccccatct ctactaaaaa aaaaaaaaaa 38400 aaaattagcc ggggtggtgg cttatgcctg aaatcccagc tactcaggag gctgaggcag 38460 gagaatcgct tgaacccagg aagcagaggt tgcagtgagc caagatcgca ccattgcact 38520 ccagcctagg caacaagagt gaaactccat ctcaaaaaaa aaaaaaaaga gctgaatctt 38580 ggctgggcag gatggctcgt gcctgtaatc ctaacgcttt ggaagaccga ggcagaagga 38640 ttggttgagt ccacgagttt aagaccagcc tggccaacat aggggaaccc tgtctctatt 38700 tttaaaataa taatacattt ttggccggtg cggtggctca tgcctgtaat cccaatactt 38760 tgggaggctg aggcaggtag atcacctgag gtcagagttc gagaccagcc tggataacct 38820 ggtgaaaccc ctctttacta aaaatacaaa aaaaaaaaaa aattagctgg gtgtggtagc 38880 acatgcttgt aatcccagct acttgggagg ctgaggcagg agaatcgctt gaaccaggga 38940 ggcggaggtt acaatgagcc aacactacac cactgcactc cagcctgggc aatagagtga 39000 gactgcatct caaaaaaata ataattttta aaaataataa atttttttaa gcttataaaa 39060 agaaaagttg aggccagcat agtagctcac atctgtaatc tcagcagtgg cagaggattg 39120 cttgaagcca ggagtttgag accagcctgg gcaacatagc aagacctcat ctctacaaaa 39180 aaatttcttt tttaaattag ctgggtgtgg tggtgtgcat ctgtagtccc agctactcag 39240 gaggcagagg tgagtggata cattgaaccc aggagtttga ggctgtagtg agctatgatc 39300 atgccactgc actccaacct gggtgacaga gcaagacctc caaaaaaaaa aaaaaaagag 39360 ctgctgagct cagaattcaa actgggctct caaattggat tttcttttag aatatattta 39420 taattaaaaa ggatagccat cttttgagct cccaggcacc accatctatt tatcataaca 39480 cttactgttt tcccccctta tgatcataaa ttcctagaca acaggcattg taaaaatagt 39540 tatagtagtt gatatttagg agcacttaac tatattccag gcactattgt gcttttcttg 39600 tataactcat tagatgcttg tcagacctct gagattgttc ctattatact tattttacag 39660 atgagaaaat taaggcacag agaagttatg aaatttttcc aaggtattaa acctagtaag 39720 tggctgagcc atgattcaaa cctaggaagt tagatgtcag agcctgtgct ttttttttgt 39780 ttttgttttt gttttcagta gaaacggggg tctcactttg ttggccaggc tggtcttgaa 39840 ctcctaacct caaataatcc acccatctcg gcctcctcaa gtgctgggat tacaggtgag 39900 agccactgtg cctggcgaag cccatgcctt taaccacttc tctgtattac atactagctt 39960 aactagcatt gtacctgcca cagtagatgc tcagtaaata tttctagttg aatatctgtt 40020 tttcaacaag tacatttttt taaccctttt aattaagaaa acttttattg atttattttt 40080 tggggggaaa ttttttagga tctgattctt ctgaagatac cgttaataag gcaacttatt 40140 gcaggtgagt caaagagaac ctttgtctat gaagctggta ttttcctatt tagttaatat 40200 taaggattga tgtttctctc tttttaaaaa tattttaact tttattttag gttcagggat 40260 gtatgtgcag tttgttatat aggtaaacac acgacttggg atttggtgta tagatttttt 40320 tcatcatccg ggtactaagc ataccccaca gttttttgtt tgctttcttt ctgaatttct 40380 ccctcttccc accttcctcc ctcaagtagg ctggtgtttc tccagactag aatcatggta 40440 ttggaagaaa ccttagagat catctagttt agttctctca ttttatagtg gaggaaatac 40500 cctttttgtt tgttggattt agttattagc actgtccaaa ggaatttagg ataacagtag 40560 aactctgcac atgcttgctt ctagcagatt gttctctaag ttcctcatat acagtaatat 40620 tgacacagca gtaattgtga ctgatgaaaa tgttcaagga cttcattttc aactctttct 40680 ttcctctgtt ccttatttcc acatatctct caagctttgt ctgtatgtta tataataaac 40740 tacaagcaac cccaactatg ttacctacct tccttaggaa ttattgcttg acccaggttt 40800 tttttttttt ttttttggag acggggtctt gccctgttgc caggatggag tgtagtggcg 40860 ccatctcggc tcactgcaat ctccaactcc ctggttcaag cgattctcct gtctcaatct 40920 cacgagtagc tgggactaca ggtatacacc accacgcccg gttaattgac cattccattt 40980 ctttctttct ctcttttttt tttttttttt tgagacagag tcttgctctg ttgcccaggc 41040 tggagtacag aggtgtgatc tcacctctcc gcaacgtctg cctcccaggt tgaagccata 41100 ctcctgcctc agcctctcta gtagctggga ctacaggcgc gcgccaccac acccggctaa 41160 tttttgtatt tttagtagag atggggtttc accatgttgg ccaggctggt cttgaactca 41220 tgacctcaag tggtccaccc gcctcagcct cccaaagtgc tggaattaca ggcttgagcc 41280 accgtgccca gcaaccattt catttcaact agaagtttct aaaggagaga gcagctttca 41340 ctaactaaat aagattggtc agctttctgt aatcgaaaga gctaaaatgt ttgatcttgg 41400 tcatttgaca gttctgcata catgtaacta gtgtttctta ttaggactct gtcttttccc 41460 tatagtgtgg gagatcaaga attgttacaa atcacccctc aaggaaccag ggatgaaatc 41520 agtttggatt ctgcaaaaaa gggtaatggc aaagtttgcc aacttaacag gcactgaaaa 41580 gagagtgggt agatacagta ctgtaattag attattctga agaccatttg ggacctttac 41640 aacccacaaa atctcttggc agagttagag tatcattctc tgtcaaatgt cgtggtatgg 41700 tctgatagat ttaaatggta ctagactaat gtacctataa taagaccttc tgtaactgat 41760 tgttgccctt tcgttttttt ttttgtttgt ttgtttgttt ttttttgaga tggggtctca 41820 ctctgttgcc caggctggag tgcagtgatg caatcttggc tcactgcaac ctccacctcc 41880 aaggctcaag ctatcctccc acttcagcct cctgagtagc tgggactaca ggcgcatgcc 41940 accacacccg gttaattttt tgtggtttta tagagatggg gtttcaccat gttaccgagg 42000 ctggtctcaa actcctggac tcaagcagtc tgcccacttc agcctcccaa agtgctgcag 42060 ttacaggctt gagccactgt gcctggcctg ccctttactt ttaattggtg tatttgtgtt 42120 tcatctttta cctactggtt tttaaatata gggagtggta agtctgtaga tagaacagag 42180 tattaagtag acttaatggc cagtaatctt tagagtacat cagaaccagt tttctgatgg 42240 ccaatctgct tttaattcac tcttagacgt tagagaaata ggtgtggttt ctgcataggg 42300 aaaattctga aattaaaaat ttaatggatc ctaagtggaa ataatctagg taaataggaa 42360 ttaaatgaaa gagtatgagc tacatcttca gtatacttgg tagtttatga ggttagtttc 42420 tctaatatag ccagttggtt gatttccacc tccaaggtgt atgaagtatg tattttttta 42480 atgacaattc agtttttgag taccttgtta tttttgtata ttttcagctg cttgtgaatt 42540 ttctgagacg gatgtaacaa atactgaaca tcatcaaccc agtaataatg atttgaacac 42600 cactgagaag cgtgcagctg agaggcatcc agaaaagtat cagggtagtt ctgtttcaaa 42660 cttgcatgtg gagccatgtg gcacaaatac tcatgccagc tcattacagc atgagaacag 42720 cagtttatta ctcactaaag acagaatgaa tgtagaaaag gctgaattct gtaataaaag 42780 caaacagcct ggcttagcaa ggagccaaca taacagatgg gctggaagta aggaaacatg 42840 taatgatagg cggactccca gcacagaaaa aaaggtagat ctgaatgctg atcccctgtg 42900 tgagagaaaa gaatggaata agcagaaact gccatgctca gagaatccta gagatactga 42960 agatgttcct tggataacac taaatagcag cattcagaaa gttaatgagt ggttttccag 43020 aagtgatgaa ctgttaggtt ctgatgactc acatgatggg gagtctgaat caaatgccaa 43080 agtagctgat gtattggacg ttctaaatga ggtagatgaa tattctggtt cttcagagaa 43140 aatagactta ctggccagtg atcctcatga ggctttaata tgtaaaagtg aaagagttca 43200 ctccaaatca gtagagagta atattgaaga caaaatattt gggaaaacct atcggaagaa 43260 ggcaagcctc cccaacttaa gccatgtaac tgaaaatcta attataggag catttgttac 43320 tgagccacag ataatacaag agcgtcccct cacaaataaa ttaaagcgta aaaggagacc 43380 tacatcaggc cttcatcctg aggattttat caagaaagca gatttggcag ttcaaaagac 43440 tcctgaaatg ataaatcagg gaactaacca aacggagcag aatggtcaag tgatgaatat 43500 tactaatagt ggtcatgaga ataaaacaaa aggtgattct attcagaatg agaaaaatcc 43560 taacccaata gaatcactcg aaaaagaatc tgctttcaaa acgaaagctg aacctataag 43620 cagcagtata agcaatatgg aactcgaatt aaatatccac aattcaaaag cacctaaaaa 43680 gaataggctg aggaggaagt cttctaccag gcatattcat gcgcttgaac tagtagtcag 43740 tagaaatcta agcccaccta attgtactga attgcaaatt gatagttgtt ctagcagtga 43800 agagataaag aaaaaaaagt acaaccaaat gccagtcagg cacagcagaa acctacaact 43860 catggaaggt aaagaacctg caactggagc caagaagagt aacaagccaa atgaacagac 43920 aagtaaaaga catgacagcg atactttccc agagctgaag ttaacaaatg cacctggttc 43980 ttttactaag tgttcaaata ccagtgaact taaagaattt gtcaatccta gccttccaag 44040 agaagaaaaa gaagagaaac tagaaacagt taaagtgtct aataatgctg aagaccccaa 44100 agatctcatg ttaagtggag aaagggtttt gcaaactgaa agatctgtag agagtagcag 44160 tatttcattg gtacctggta ctgattatgg cactcaggaa agtatctcgt tactggaagt 44220 tagcactcta gggaaggcaa aaacagaacc aaataaatgt gtgagtcagt gtgcagcatt 44280 tgaaaacccc aagggactaa ttcatggttg ttccaaagat aatagaaatg acacagaagg 44340 ctttaagtat ccattgggac atgaagttaa ccacagtcgg gaaacaagca tagaaatgga 44400 agaaagtgaa cttgatgctc agtatttgca gaatacattc aaggtttcaa agcgccagtc 44460 atttgctccg ttttcaaatc caggaaatgc agaagaggaa tgtgcaacat tctctgccca 44520 ctctgggtcc ttaaagaaac aaagtccaaa agtcactttt gaatgtgaac aaaaggaaga 44580 aaatcaagga aagaatgagt ctaatatcaa gcctgtacag acagttaata tcactgcagg 44640 ctttcctgtg gttggtcaga aagataagcc agttgataat gccaaatgta gtatcaaagg 44700 aggctctagg ttttgtctat catctcagtt cagaggcaac gaaactggac tcattactcc 44760 aaataaacat ggacttttac aaaacccata tcgtatacca ccactttttc ccatcaagtc 44820 atttgttaaa actaaatgta agaaaaatct gctagaggaa aactttgagg aacattcaat 44880 gtcacctgaa agagaaatgg gaaatgagaa cattccaagt acagtgagca caattagccg 44940 taataacatt agagaaaatg tttttaaaga agccagctca agcaatatta atgaagtagg 45000 ttccagtact aatgaagtgg gctccagtat taatgaaata ggttccagtg atgaaaacat 45060 tcaagcagaa ctaggtagaa acagagggcc aaaattgaat gctatgctta gattaggggt 45120 tttgcaacct gaggtctata aacaaagtct tcctggaagt aattgtaagc atcctgaaat 45180 aaaaaagcaa gaatatgaag aagtagttca gactgttaat acagatttct ctccatatct 45240 gatttcagat aacttagaac agcctatggg aagtagtcat gcatctcagg tttgttctga 45300 gacacctgat gacctgttag atgatggtga aataaaggaa gatactagtt ttgctgaaaa 45360 tgacattaag gaaagttctg ctgtttttag caaaagcgtc cagaaaggag agcttagcag 45420 gagtcctagc cctttcaccc atacacattt ggctcagggt taccgaagag gggccaagaa 45480 attagagtcc tcagaagaga acttatctag tgaggatgaa gagcttccct gcttccaaca 45540 cttgttattt ggtaaagtaa acaatatacc ttctcagtct actaggcata gcaccgttgc 45600 taccgagtgt ctgtctaaga acacagagga gaatttatta tcattgaaga atagcttaaa 45660 tgactgcagt aaccaggtaa tattggcaaa ggcatctcag gaacatcacc ttagtgagga 45720 aacaaaatgt tctgctagct tgttttcttc acagtgcagt gaattggaag acttgactgc 45780 aaatacaaac acccaggatc ctttcttgat tggttcttcc aaacaaatga ggcatcagtc 45840 tgaaagccag ggagttggtc tgagtgacaa ggaattggtt tcagatgatg aagaaagagg 45900 aacgggcttg gaagaaaata atcaagaaga gcaaagcatg gattcaaact taggtattgg 45960 aaccaggttt ttgtgtttgc cccagtctat ttatagaagt gagctaaatg tttatgcttt 46020 tggggagcac attttacaaa tttccaagta tagttaaagg aactgcttct taaacttgaa 46080 acatgttcct cctaaggtgc ttttcataga aaaaagtcct tcacacagct aggacgtcat 46140 ctttgactga atgagcttta acatcctaat tactggtgga cttacttctg gtttcatttt 46200 ataaaagcaa atccaggtgt cccaaagcaa ggaatttaat cattttgtgt gacatgaaag 46260 taaatccagt cctgccaatg agaagaaaaa gacacagcaa gttgcagcgt ttatagtctg 46320 cttttacatc tgaacctctg tttttgttat ttaaggtgaa gcagcatctg ggtgtgagag 46380 tgaaacaagc gtctctgaag actgctcagg gctatcctct cagagtgaca ttttaaccac 46440 tcaggtaaaa agcgtgtgtg tgtgtgcaca tgcgtgtgtg tggtgtcctt tgcattcagt 46500 agtatgtatc ccacattctt aggtttgctg acatcatctc tttgaattaa tggcacaatt 46560 gtttgtggtt cattgtctcc ttaaattaga ctgtaagcac cttgatggaa ctcatactac 46620 cttttatttc acacacacgc acacgcgcac acacagccta cacatacact gcctagctca 46680 ttgtagcata ctaaatactg attttaatga ataagctaaa ccttcgaaac ccatttgcta 46740 atcccagcac tttgggaggc caaggtgggt ggatcacctc aggtcagaag tttgagacca 46800 gcctggccaa catggtgaaa ccccacatct actaaaaata caaaaattag ctgggcgtgg 46860 tggccaatgc cttgtaatcc cagctattct ggaggctgag acaggagaat cgcctgaacc 46920 tgggaggcgg aggttgcact gagctgggat tgtaccactg cactccagcc tgggtgacaa 46980 agtgagactc catctcaaaa acaaacaaac aaaaacacat catttcccct atagcaaaaa 47040 catgacggca cttactgtat caagagaggt gagaaaaagg agccacagca ggatgattca 47100 agggactctg catagctcca ttttaagaat atgcctactg caggtcagag aaggtaagca 47160 aactgcctaa ggccacacag ccaggtacag aactctcacc aatattattg ccagcaatcg 47220 caattttggt gtttattctt ggtaccaagt tggagactat agggttctct tcctaataga 47280 gaccatctag cctttcactg ttttgtggat acttctttct cttcttcttt ttttttttcc 47340 cttttaaaat ctagttattt ttttcttttt ggtttctttg acacagggtc tcttactctg 47400 ttacccaggc tggaatggag tagtgcagtc atggttcact gtagctttga cttcctgggc 47460 tcaagcgatc ctcctacctc agcttcccga gtagctggga ccacaggcgc ccaccaacac 47520 ctccagctaa tttttaagtt tttactagag acaacatctc actatgttgc ccaggctggt 47580 ctcaaaatcc tgggctcaag tgatcccacc tcagccttcc aaaatgctgg gattacaggt 47640 gtgtgcacca cgcctggcct attttttttt taattgctca taaatcatct tttttcttta 47700 aaaaaaagaa agatgggagg ctaaagcagg agaatcactt gaacccagga ggcggaggtt 47760 gcagtgagct gagatcatgc tgctgctctc cagcctgggc aacaagagtg aaactccatc 47820 tcaaaaaaaa aaaaaaagaa agtacacaat tttactttct ggacctaatg gtcaaggcca 47880 ataatttggt cacctatgaa ataaataaaa gctttaccat atatatgacc atttgataat 47940 gtaatatgaa atgtttatgt actaaaggca gaatagtcta gaaaaaacat tctgtatcac 48000 aacgtctaaa aatgaatatc atcttcatca tagaaccagg ctctttctcc taattttttt 48060 ttttgagatg gagttttgct ctgtcaccca ggctggaatg cagtggcaca attttggctc 48120 actgcaacct tcagctccca ggttcaggat caagtgattt tcgtgcttca gccttctaag 48180 tagctgggat tacaggtgac tgccaccaca cccagctcat ttttttgtat ttttttagta 48240 gagagagggt ttcaccatgt tggccaggct cgtctcgaac tcctgacctc aaataatcca 48300 cccgtctcag cctcccaaag tgctgagatt acaggcgtga gccaccaggc ctggcctcct 48360 aatttttatt tgtagaagtg gcaccaaaat tttccaagtt ctcatgcaaa aattcaggct 48420 catctcagtt tatttttttc atttatttat ctcccactaa attgacaact tctaataatt 48480 aggttggttc tttgtattcc cagcacaggg ttctatgcag aatacacaca cagcagttgc 48540 tggcaataat attggtgaga gttctgtact gggctatgtg atcttagaca gtttgcttat 48600 gttctctgac ctgccgtagg cacattctta aaatgaagct gttcagaccc cctcgattca 48660 tcctgctgtg gcttcttttt cccacctaaa tcttaaatac ccttttagct gctagtaagt 48720 gaatgatgtt tttttatgaa ctttctgaag tcagattaga tgaagttgag aaaagcctga 48780 tattcttata aagttatata tgtgcatcat agaaaactta gaaaatacag ataaacaaaa 48840 atcatccatg gacgaacctt gaagacattg tgttaactga aataaaccgg acaccaaagg 48900 acacatgtta tatgcttcca cttatatgag atacctagaa tagttacatt tggttactct 48960 gggtacattg cctatagata agccttgctc cacaaggagc agttaaaaaa aaaaaaaaga 49020 taaattcata ggatggaagg tagaatagtg gttactaggg acttggggag ggggaaatgg 49080 ggagttactg tttgatgagt gcagatttca gtttgggatg atgaaaaagt tctggagata 49140 gatagtggca atggtaacac aacagtgtga aaataatgcc actgaactgt acacttaaaa 49200 tgattaaaat gataagttaa ttgtaatttg tgttatccag aaatggttag caatttattg 49260 gtgtatattc ttttagtatt cctgtgtgtg cacaggggtg cttgtatata ctttatcttt 49320 aaaatatatc caggaagcta ggcacagtgg cttacacctg taatcccagc actttgggag 49380 ggtgaggcag gaagattgcc tgagccccgg aggtcaaggc tgcagtgagt tgtgatcacg 49440 ctactgcact ctgttctggg caacccctgt ctgggaaaaa aaaaaaaatt agtgaggctt 49500 agtggtgcac acctgtagtc tcagctactt gagtggctgg ggtaggattg cttgatccca 49560 gcaagttgag gccgtggtga gccatgatgg tgccactgca ctccatcctg ggtgatatgg 49620 tgagaccctg tctcaaaaac aagaaatcca gataattctg tgcattataa tctagctttt 49680 actggatcat taaaattctt ttttcttttt tttttttttt ttctgagatg gagtttcact 49740 cttgttgccc aggctggagt gcagtggtgt gaccttggct caccgcatcc tctgcctccc 49800 gggttcatgc gattctcctg cctcagcctc ccgagtagct gggattacag gcatgtgcca 49860 ccatgcccag ctaactttgt atttttagta gagacagggt ttctccatgt tgaccaggct 49920 ggtctcaaac tcctggcctc aagtgatcca cccacctcgg cctcccaaag tgctggggtt 49980 acaggcgtga gccaccgcac tcagcctggg tcgttaaaat tcttaagtga cttcattttt 50040 aattactata tgggattcta tctttccagt gtatcatgat ttatttgacc tattgctgaa 50100 tgttggaggt ttcagggtaa gaggcacagt ttgctattat gtacatcact atagtggcat 50160 cctgatagct aaatatttgc ctacatccct gattatttcc ttagtctaaa ttactgggac 50220 taggattttg gtgtttgata catgttacta aattgttttt tagaaagatt aaaccagttt 50280 atgctcttcc agcccctgtg gtatatgata gttcccattt tcctgtacct tgccaacact 50340 gggtgatatc cagttttaaa atctaaatct tgcattgcta tgagaactac aattagagaa 50400 ggcttatctt ctactgccca ttctctgtac agagcaaatc cctctagacc tgaagcccct 50460 tggagttgtc aagaaacctt tgagatgact ccccactctg tatctgagct gtcaccagta 50520 ttctccactt cttcaggatt gccatggcaa ctaaattgat gaaaagattt aggaggcctt 50580 ttctctcttt gcaattccta tgatcctttt tgaatgtggg tttgggactc tgtcaatata 50640 cccatcatct aattctgtcc attgtgtttt aaagtttaag gttgcaattt ctgattacat 50700 ctgccttagc catactgtat tatatttgac attcaatata caatgtcctt gtttttctgt 50760 atttctaatc ttattcccag agatgtgtct atttgttcag gattcatttt gcaacgtgtt 50820 tttactaagc atctacccaa aaccgttgaa gtcagatttc aggctgtctt acgtctaaag 50880 tagcacaggc aggaaaaact attgaagtgg gatttttttt tccctttttg tactgaaccg 50940 agaaaaagta tatagatgat agagaattcc taatttggta tcattgatat ctgggttttt 51000 gtttgttttt acagaagact gattaactat acttatttat taatttatct tctcattaat 51060 aaacacttgc tgagtgctta ctgtctgcta ggcattaggg agacaaatat gattaaggga 51120 agcttcctcc tatcaaggtc atgtgttcca tttgggtata ctaatgcatt agcaatgtaa 51180 atcaagtagt gagagatcat ctgttcccga taggagatgg attattggtg gggacttctg 51240 tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg tgtgtgtatg tatgtgataa aataaatata 51300 ggaaatgtta attatagatt ctaagtagta gatatataaa cactcattgc aaagttgctt 51360 caagttttct gtatatttga aaatattcac aacatgtcga caaaactagc atgataaagc 51420 cactatttgt gctaagactt cagcttgtat ctggattagg cttattatgt agtagtagga 51480 acattagaaa tagttttaac tcattaaata cacatgtttt atgggaaggt tttatatata 51540 tatttatatg taatgaatgt gaacaaacaa gggtcagata tacactctgc ttccctccag 51600 accagttccg gctgctctgc tgcacatttc aggagtctta ttagaattag ccacattctg 51660 cccacttgcc cttacttctc atatttcaca actcctcctg gtggggactt aaggagacat 51720 tcaaactagg ccttgaaaga tgagaatttt tccaagtgga aaaagaggag tggcagcaag 51780 taaggtaaag gtacagagtc atggaattcc caggaaacgt aaagttgtca tgtgttatag 51840 gaaaacaact tgtgtgaggg gtgttgggag aaatgagaga taataccagg gtataaaggg 51900 ccttttgaat gctatgttga ggaattttat cctaatggca gtaatgacta acaattatat 51960 agtgttcaaa aagtataaat cagcagtggt ataccactaa gggttttttt cttttctttt 52020 tttttttgag acagagtttt gctctgttgc ccaggctgga gtgccgtggc acgatctcag 52080 ctcactgcac ttccgccacc tgggttcaag tgattcttct gcctcagcca gtgtttcact 52140 gtgatggcca ggatggagca ctaagggtct ttatggaaga aaaagacatg ataaacaagg 52200 cttttaggga acttctacag taatgtagct gtattaaaag tagagatcag agcagcatag 52260 tagaagtaga aggctagagc taattgaagg agcacttcag aattagaatc aagaagtctt 52320 agaaacctat tggttttatt ctccctaatg tatttggcca cttacctgct ggggaatttg 52380 tctaagttat aaaaaataat tcctttggga aacccaaagg aaagttatct attaataatt 52440 accccactac tttttctgat ttatgtaatg gccacgtaga ggttagatgt gatggttgtg 52500 acagtagtga ctaatacagc ctgtgaagca ttttggtcag atatctatgt gctttcattc 52560 caggttgact gaggcaagac tttggctagg gtttgatcag tgatgtaact actcacgagt 52620 accacgtggt ggcaatggca ttgctgcaga ccttggcagc aaagcagtgt tagagtagca 52680 gtagaaacct ttgtgaagct aggaatacat tttctggtca taaaaacctc ctgaaaattg 52740 tgaactcagt gtagcaggag aaagaagatg gcttgttttt agtaaagggc aaagtcattt 52800 ttaaggatca gaagaagaaa cggagagtga aacaatgtgt tcctgcccta ctcccccact 52860 ggactttttg gcaaccattg ctgttccttc taaaagtgat ttttaaacat gtatattttg 52920 aagccaggca cagtgactca cgtctgtaat cccagcactt tgggaggccg aggcgggcag 52980 atcacctgag gtcaggagtt caagaccagc ctggccaaca tggtgaaacc ccgtctctac 53040 taaaaataca aaaattaggc caggtgtggt ggctcacgcc tgtaatccca gcactttggg 53100 aggccgaggc gggaggatca tgtggtcagg agatccagac catcctggct aacacggtga 53160 aacaccattt ctactaaaaa tacaaaaaat tagctgggca tggtggcggg cgcctgtaat 53220 cccagctact caggaggctg aagcagaaga atggcttgaa cctgggaggc ggagcttgca 53280 gtgaaccaag attgcgccac tgcactccag cctgggcaac aaagtgagac tccgtctcaa 53340 aaaaaaaaaa aaaaattagt cgggcatggt aacaggtgcc tgtaatccca gctacttgag 53400 aggctgaggc agggagaatt gcttgaacca ggtaggcgga ggttgcagtg agccaagatc 53460 gcaccactgc actccagcct ggggcaacag agcaagactg tctcaaaaaa aataaataaa 53520 taaaataaat tcttaagaag gatattttgg aaaactcctt acatacctaa attctttgtt 53580 tatcaaatac ttggacttag cacactcttc tttgaaatgg accaataaac aacaggagcc 53640 cataagcaaa aagaactcat tattttaaaa acagtaacta tccttacagg ctttctcagg 53700 gctctttctg ttggatcctt ccctctcaca ggtccttgct aatgatctct aggtggacac 53760 attctagatg agatgtccct gtctagaatg gcagcaccat gagggctata tcctcagtac 53820 taggacagcg cctggtgctt aatagatagt aaatagttgt ctaattaact gagcaaacag 53880 atagattcat gaattagctt tttgcttttt ctgttagaaa ctaaaggttc aggtcaggca 53940 caatggcgca tgtctctaat cccagcactt tgggaggccg aggcgggctg atcacttgag 54000 gtcaggagtt caagaccagc ctggccaaca tagtaaaacc ctgtttctac aaaaattacc 54060 aaaattagcc gggcgtcttg gcaagcacct gtaatgccag ctacttgaga ggctgaggtg 54120 ggagaatcgc ttgaacctgg gaggaagagg ttgcagtgag ccgagatggt gccaacctgg 54180 gtgacagagg gagacttaaa aaaaaaaaga aagaaagaaa gaaaagaaac taaaggttca 54240 aagaatccca gaaaaggaag agtcctcaca agccagtaat ctaggcagga ttactgatag 54300 tatttttata tttgttgtat ttttataaaa tgccatagat agagggcttt tttcaacatt 54360 acatcagtct aaaaatcaca catttttata tgaactaacc taaatgtctg atgaatctca 54420 caacaccaag tctttgaaat gtgcccatat aaataaaatg ttaacagatt catgctaatt 54480 ttaaatatcg atagtgttta aatgccttaa ttattttttc actccctagc tttaaaagaa 54540 aataaccaac ttcaaaagga catcacaata acatcaagtc tatttggggg aatttgagga 54600 ttttttccct cactaacatc atttggaaat aatttcatgg gcattaattg catgaatgtg 54660 gttagattaa aaggtgttca gctagaactt gtagttccat actaggtgat ttcaattcct 54720 gtgctaaaat taatttgtat gatatatttt catttaatgg aaagcttctc aaagtatttc 54780 attttcttgg tgccatttat cgtttttgaa gcagagggat accatgcaac ataacctgat 54840 aaagctccag caggaaatgg ctgaactaga agctgtgtta gaacagcatg ggagccagcc 54900 ttctaacagc tacccttcca tcataagtga ctcttctgcc cttgaggacc tgcgaaatcc 54960 agaacaaagc acatcagaaa aaggtgtgta ttgttggcca aacactgata tcttaagcaa 55020 aattctttcc ttccccttta tctccttctg aagagtaagg acctagctcc aacattttat 55080 gatccttgct cagcacatgg gtaattatgg agccttggtt cttgtccctg ctcacaacta 55140 atataccagt cagagggacc caaggcagtc attcatgttg tcatctgagt acctacaaca 55200 agtagatgct atggggagcc catggaagat acatggtata caacatagct cttgctctat 55260 tggaagctaa gtggaatggg agaaattggt gacaggcaac cccataattt cagaaagcta 55320 tgaaaaagta ctcagacata ttccttataa cactggtgtc acatcacaaa gacctattta 55380 atgtgcttct gatttatagg gagagacatc ctatacttca ggaactgcac tttgatccac 55440 agaaagccta gtgatgtaga gctcctgtta gttcaaaagg aaaagaaaag aacaacacag 55500 aaagcctaat tatgcaatag agtcaagtgc tttatagcaa tgttacagtt atcaaaaaaa 55560 atccagatgg acctctgaga ggatgccatt ggagtaacca ggcagatgca gttgatcaga 55620 gctgacttcc tataagaagt gagcactgag ctgaggaata atggcataaa tgaaggaaag 55680 tgagatggaa atttgagttt ttaattggaa agacaataca tcaggcagat ttttaaatag 55740 gggcaaacaa acagacacat aggagatgct aggcatgggg tccccactag gatgctgctt 55800 agaaacatgc aggggtggtg agtactccca aagtacactt cattcctagc tcagtgattc 55860 ttatctgagt gttaaagttc cttcttcagc accccgttcc acagtccaac tgggaacttt 55920 aagacctttc ttggagtctt tctaggaact caagtctgct acttatacag aacagtggct 55980 ttggtcccca gttgtgcctt gcagtatttt tgtgttcagg aagaaacagt agctcttgga 56040 taaagaagct agctagaaac tctgttgcta tggcagtgct tcaaaatgta tttccttaaa 56100 tgctttcttt gtaactatct tcatttagtt catctctcag ataatgagag atcagagtcc 56160 catccccagt ataatactct tctttagggt actttcacca tcttcagtct aaacacagac 56220 tagactttca attataatgt gtaagattta aaatgttatt attgtgtgac tttgaatatc 56280 tgtgtaaatc tactatctcc tctttggtat atacgtgtgt ttattttttt ctggagatct 56340 gtaactgaaa tgcttaattt ctgaattgtt ttggatatca caacttaata ccaacataag 56400 ttttgagcct ttttctccct aaatctggtg tgagtctaac tgaaactcaa atgaactttt 56460 taaaaataat tttttctttt ctttaatttt ttttttaagt agagacaggg acgcactgtt 56520 aactaggctg gtcttgaact cctgatcttg agccatcctc cccgacctga gcctcacctt 56580 atagagaggg tcttgctctg ttgcccaagc tggagggcag tggcataatc acagctcact 56640 gcagcctctc gacctcctca agcgatcctc ctgccttagc ctcccaagta gctgggacta 56700 taggcgtcca ccaccatacc cagctaattt ttttttttat tttttgtaga gacaaggtct 56760 ccctatgttg cccaagttgg tctcaaactc ctggactcaa gcagtcctct cacctcaggg 56820 tcccaaagtg ctggggttac aggtgtgagc catggcacct ggccagaact tctagtaaaa 56880 agaatattgt tgccgggtac ggtggctcac gcctgtaacc ccagcacttt gggaggccaa 56940 ggcaggcgaa tcacctgagg tcgggagctc gagaccagcc tgaccaacat ggagaaacca 57000 catctctact aaaactacaa aaaattagcc gggcgtggtg gcacatgcct gtaatcccag 57060 ctacttggga gctacggtgc ctggcctagt ttattatttc ttaatatctg ttgtcttcca 57120 gtgtcttcct taattcttca caataccctg tacaatgctt agcacacagt gggcagtctg 57180 taagtttatt aaatgtttgg tgtggcccat acttcctatc cacaaagaat gtaacatgtt 57240 aagacatcta gatgagggaa tgatttaaga ggaactacaa taatattctg aaacttggac 57300 tctggatctc tgcatttaga ctttcctaaa ccagccagca agtagatcat catgtcacaa 57360 ggcttaggtt gggcttgctg ttcagagaat gaattaagga ttaaggagaa aaaaaagcag 57420 aaaggttttg ctctgttttt caggttctat tgagttgtta acttctaaca agttatctta 57480 tttgcttcat tgcatgaggc ccattgtagt aagaagagga atttatatgc taaatgttct 57540 ggtgatagaa tgacttttct ttttttttac agtccaaagg tctttttttt ttttttttaa 57600 cacctattat gccatgaatt catagggaat aggttccagc tgctcaggct ccttcccatt 57660 ggttctcaca aagtgtgctt ctctgggtgg agcaggctgg tgcttcagtt gaacccacgt 57720 acctttctct ttggcttctt tctttttctg atcattttcc ttcacgcgtt tcaggaagct 57780 gtcttggctc ttagagtgtt taatgtgctc aatacgcaca ttaattctct tggcaagaat 57840 cttgccctta acttgtttac agcgatgcca acagcatgct gggtcacgtt gtagactttt 57900 ccagttttgc catggtaaca cttgtggggc attccttttt gaacagtacc cgttcccttg 57960 atgtctacaa tttcaccttt cttacagatt cgcatataca tggccaaagg aacaactcca 58020 tgttttctaa aaggcctaga gaacatatat caggtgcctc tcctctttcc ctttgtgttc 58080 gtcattttgg caaattactg aaagatggtg gttctggcca aaaggaggaa tgacttttta 58140 atagctgtgt ttgtatctga gccttccctc tgcctttcat tttttttgtt ttgttttgtt 58200 ttgtttttgt ttgagatgaa gtttcacttt tgttgcccag gctggagtgc aatggtgtga 58260 tttcggctca ttacaatgtc cgcctcagcc tcctgggtag ctgggattac aggcacccgc 58320 caccacgccc agctaatttt tgtattttta gtagagacag ggtttcacca tgttggccgg 58380 gctggtctca aactcctgac ctcaggtgat ctgtccacct cggcctctca aagtgctggg 58440 attgtaggcg tgagccacat cacctggcca cttttttaac tctttccaat ggttaattcc 58500 gtttgatatg gttccttgga acttgcacat taccctttat caattatcac cctgtattgg 58560 gggtggggag gatgatacct ctcttcatag ttagatccta cttactttca acagagttct 58620 taacaatcct agaaactcac aggtccagaa aagacaagca taaaggaaac tataaataat 58680 gcatttgaag actaactcag gaaatcaatg attatttccc cccaggctac ccagtgtctt 58740 aaaaaaacag tttaattaat acaatctttt gtttcaattt tctacctata tttatggctt 58800 ttagcttttc taataaaagc tcaaaatgaa ttacagtcat cagtgacttt ttaatgaata 58860 gaagactttt gcaattttta actatttgtt tttacttatt aaatatttcc gccttggcca 58920 ggcatggtgg ctcacgccta taatcccagc actgtgagat gccaaggcag gaggatcact 58980 tgagtttaag agttctagac caggctgggt atggtggctc atgcctataa tcccagcact 59040 ttgtgaggcc aaggttggcg gatcacctga ggtcaggagt ttaagaccag cctggccaac 59100 atggtaaaac cccatctcta caaaaaatac aaaaattagc caaggggtgg tggtgggcac 59160 ctataatccc atcttcttgg gaggctaagg caggagaatc gcttgaacct ggaggcagag 59220 gttgcagtga gccgagatca tgccactgta ttccagcctg ggtaacagag caagactctg 59280 tctcaaaaaa aaaaaaaagt ttgaaaccag cctggtcaac acagcaagac acccatctcg 59340 ttgaaaaata acggtcgggc gcagtggctc acgcctgtaa tcccatcact ttgggaggcc 59400 gaggcaggca gatcacctga ggtcgggagt tcgagaccag cgtgaccaac atggagaaac 59460 cccatctcta ctaaaaatac aaaattagtt gggcgaggtg gtgcatacct gtaatcccaa 59520 ctacttggga ggctgaggca ggagaacagc ttgaacctgg gaggcagaga ggttgtggtg 59580 agccaagatc atgccattgc actgcagcct gggcaacaag agcaaaactc catctcaaaa 59640 aaaataaata aataaaaata aataaataag tacttctgcc tttaagccac ttcctagaag 59700 gcagtggcac aaagtgatac atttggagga gtaaatatat tacaaaatga attaggctgg 59760 gcgcagtggc tcatgtctgt aatccccgca ctttgggagg ccaaggcggg tggatcactt 59820 gaggtcagga gttcgagact agcctgatca acagggtaaa atcccatctc tactaaaaat 59880 accaaaaaaa ctagctgggc gtggtggcag gcacctgtaa tgtcagctac taggaaggct 59940 gaggcaggag aatcgcttga acccaggagg tggaggttgc agtgagccaa gattgcacca 60000 ttgcacttca gcttgggcaa cagagtgaga ctccgtctca aaaaaaaaaa aagaactaac 60060 atgccagaac tttgccttca gtatgttttg tgatttttcc cttcttgtgc catttcatca 60120 ttagttccat gtattattta agatttctta tcaaccagca ccttgggatt tttttgtgta 60180 tgtgttggtt tagggggttt atttgttttt ttcttttttt tcggtaattg aaaatgtgaa 60240 gcaaaatgtc acctgttttt tctttcatgt ctgacactca tgtcttgttt acccccgaca 60300 tgcagaagct gaaatcccca tttcatacag tcttcaatgt ggaggcagta gggatggaga 60360 aaataatgta ctttgtgctc tccggtactc tttctttcct attgtctgag gggatttggg 60420 cataatttat tttgctgcag agataaaaat ttgttatata tattttttat cattcagggc 60480 caaggaatat agattttttt tttcagcctt gtctcagctg ggtgtcttta tttactctgt 60540 cttaaagtgt tccttttatt atcattatta ttttttaatc attgaattcc atttggtgct 60600 agcatctgtc tgttgcattg cttgtgttta taaaattctg cctgatatac ttgtttaaaa 60660 accaatttgt gtatcataga ttgatgcttt tgaaaaaaat cagtattcta acctgaatta 60720 tcactatcag aacaaagcag taaagtagat ttgttttctc attccattta aagcagtatt 60780 aacttcacag aaaagtagtg aataccctat aagccagaat ccagaaggcc tttctgctga 60840 caagtttgag gtgtctgcag atagttctac cagtaaaaat aaagaaccag gagtggaaag 60900 gtaagaaaca tcaatgtaaa gatgctgtgg tatctgacat ctttatttat attgaactct 60960 gattgttaat ttttttcacc atactttctc cagttttttg catacaggca tttatacact 61020 tttattgctc taggatactt cttttgttta atcctatata ggttttttga acctataaca 61080 taagctacaa catgagaaat gtgcggttag atagatatgt cccttctgaa ggtcagaaaa 61140 aaatataatg gaggtaaaac ctgaacaagc ttggaaactg atggtagact tcttcaaggc 61200 agcccttgcc ctaattaaaa ttcttgtctt tctagaaaaa gtctagctgt tgatttacca 61260 cagaaaataa taataataat tactattatt attatttttt gagacagggt cgccctgtgt 61320 cacctagatt gcagtggtgc agtcatggct cactgcatcc tccgtttttc aggctcaagc 61380 aatcctccca ccttagcctc ctgagtagct gggtccacaa gcatgcgcca cccacaccca 61440 ctaagttttt gtatttttgg tagagatgga gttttacctt gttgcccagg ctggtctcaa 61500 attcctggac tcaagtagtc cgcccgcctt gccctcccaa agccagaaaa catttagaat 61560 atctttcaga gatgtgtatt tacaccacta ttaacacagg gctgtatagc agtccagtac 61620 tggactatgt agtccagtac tattcttttc cttactggag ggccaggcgt ggtggcaggt 61680 gcctgtaatc ccagctactc aggaggctga ggcaggagaa ttgcttgaac ctgggaggca 61740 gaggttgcag tgagctggga ccgtgccatt gcactccagc ctgggcgaca gagcaagact 61800 ccgtctcaaa acaaaaaaaa aaagagagag agagcagtaa ttcaggtctc acccatcttc 61860 aatccagggg gcctagcctt agtatttgac ccatagtaag cacccaataa ttgtttaaat 61920 taattaacct ctgaggccct ttaaatctgt tgataagtat cttattttgc aaagtcctaa 61980 gcacttggaa gagcagagga actatttact gggtgtgtat gcttttctaa caatatttta 62040 tagctggctt ttgtttttag aatgaatttg aacattgaaa aggcaggcaa tagggatgat 62100 tctgtgaatt ctgctaaaac tgagtagaaa gaatgagtgt agagatgtcg acattgatca 62160 actttctatc ttcataagag atctgattct aacatatcca tttagactca agtagaatat 62220 tgtgtataga gtgagtggca gtgagtaatt tggtaaaaat ttgctgacct gcttttattc 62280 tttcctcctt tctttcttcc tttccttcct tccttccttc cgtcctttcc tttcctttcc 62340 ctcccttcct tccttctttc cttctttctt tcctttcttt cctttcttcc tttctttcct 62400 tcctcccttc cttttctttt ctttctttcc tttccttttc tttcctttct ttcctttcct 62460 ttctttcttg acagagtctt gctctgtcac tcaggctgga gtgcagtggc gtgatctcgg 62520 ctcactgcaa cctctgtctc ccaggttcaa gcaattttcc tgcctcagcc tcccgagtag 62580 ctgagattac aggcgccagc caccacaccc agctactgac ctgcttttaa acagctggga 62640 gatatggtgc ctcagaccaa cccaacccca tgttatatgt caaccctgac atattggcag 62700 gcaacatgaa tccagacttc taggctgtct tgcgggctct tttttgccag tcatttctga 62760 tctctctgac atgagctgtt tcatttatgc tttggctgcc cagcaagtat gatttgtcct 62820 ttcacaattg gtggcgatgg ttttctcctt ccatttatct ttctaggtca tccccttcta 62880 aatgcccatc attagatgat aggtggtaca tgcacagttg ctctgggagt cttcagaata 62940 gaaactaccc atctcaagag gagctcatta aggttgttga tgtggaggag caacagctgg 63000 aagagtctgg gccacacgat ttgacggaaa catcttactt gccaaggcaa gatctaggta 63060 atatttcatc tgctgtattg gaacaaacac tttgatttta ctctgaatcc tacataaaga 63120 tattctggtt aaccaacttt tagatgtact agtctatcat ggacactttt gttatactta 63180 attaagccca ctttagaaaa atagctcaag tgttaatcaa ggtttacttg aaaattattg 63240 aaactgttaa tccatctata ttttaattaa tggtttaact aatgattttg aggatgaggg 63300 agtcttggtg tactctaaat gtattatttc aggccaggca tagtggctca cgcctgtaat 63360 cccagtactc caggaggccg aggcaggtgg atcagctgag gtcaggagtt caagacctgt 63420 ctggccaaca tggtgaaacc ctgtctctac taaaaataca aaaaaattaa ctgggtgtgc 63480 tagtgcatgc ccgtaatcct agctactctg gaggctgagg cagcagaatc acttgaaccc 63540 gggaggcgga ggttgcggtg agccaagatc acaccactgc actccagtct gggtgacaga 63600 gcaagactcc atctcaaaaa atatatatat atatatatac acacatatat tttatttcaa 63660 ctgttagaca agagtccaaa ggccaaagaa taaagtttta ggccagtcct ttattagaaa 63720 atgagtcaaa tcccaaagca agttttttta tgagttaatg aatataaatg actacatatt 63780 ttatgcctta aaaatcactt ttaatgaatg gtgttttatg gcttgtaaat cagagtttta 63840 atcagtaaag aaagttttta atcctcaaaa acacgttatc ataaaagaca ctgtttggca 63900 tcaaatgtgg tatttggcca tgttcattag ggtcatttta ggaatctcat acattctact 63960 tagctatgct taattcctga taccatggca ttttctgaaa tgtttcaagg atgacatctc 64020 tgctgttttt aatttggtaa tgatatctgc tgatttatta agtgaaaaaa gtaatggtgt 64080 cattaccttg gatgaagaaa caaaaataaa gcatttgcca catttttcaa ctttgttttc 64140 ctttcttaca aaattgctat aagctcattg cccccaaatt ggacaatata gggaataaaa 64200 aagataattt ggggtggggt tagacacggg tcttgttatg ttgccgaggc tggtctctaa 64260 ctcctggcct catgcaatct tcctaccttg gcctcccaaa gtgctgggat tataggtgtg 64320 agccacttca ccaagctgag atgccacctc ttaaaagaga gaataaggac agattacagc 64380 cactgctcat gcctgtaatg tcagtacttt gggaggccaa ggtgggagaa ttgctcgagg 64440 ccaagagttc aagaccagcc tgggcaatgt agcgagacct gatctctatg aaaagggggg 64500 tgggggggaa aactagctgg ggccaggcgt ggtgggtggc ttacgcctgt aatcccagca 64560 ctttgggagg ccgaggcggg cagatcacct gagggcagga gttcaggacc aacctgacca 64620 atatggagaa accctgtctc tactaaaaat acaaaattag ccaggcttgg tggcttatgc 64680 ctgtagtccc agctactcgg gaggctgagg caggagaatc gcttgaacct gggaggcaga 64740 ggtttcagtg agctgagatc gcgccattgc actctagcct gggcaacaag aatgaaactc 64800 catctcaaaa aaaaaaaaaa tcagctggaa ggtggcaaac acctgtggtc ccagctactc 64860 aggaggctga gacaggaaga tcacttgagt ccaggaggtc aaggctgcag gtgagccatg 64920 tttgtgccac tgcactgcag cctggatgac agaccgagac ccttctcaaa aaaaaaattt 64980 ttcccggtat ttttttttgg gggggggttt aattcttgtt gcccaggctg gggtgaattg 65040 gggaattttg ggttaaggga accttcggct tcctgggttg gggggttttt cctgtttagg 65100 cttccccagt agctgggatt acaggcatgc accaccacgc ccggctaatt ttttgtattt 65160 ttagtagaga cagggtttct ccatgttggt cagactggtc tcgacctctt gacctcaggt 65220 gatccgccca ccttggcctc ccaaagtgtt gggattacag gcctgagcca ccgcacccgg 65280 cctgtactct tattctttaa taataaaata tttctgtgtt tctttagtca ttttacataa 65340 acttttattt atttatttat ttttatttat ttattttttt gagacggagt ctcgttctgt 65400 tgcccaggct ggaatgcaat ggctcaatct cagctcactg caagctctgc ctcccgggta 65460 cacgccattc ccctgcctca gcctccctag tagccgggac tacaggcgcc cgccaccacg 65520 cccagctaat tttttttttt gtattttcag tagagacagg gtttcactgt gttagccagg 65580 atggtcttga tctcctgacc tcgtgatcca cccgtctcgg cctcccaaag tgctgggatt 65640 acaggtgtga gccaccgtgc tcggcccata aacttttatt tttaaaataa tgtcatgata 65700 aataatattg cttaggtgtc tttaatatat tagtaacatt tctgttttat tgtacatcaa 65760 catttatatt caaattaatg ggtgaagagt actccattgg actaggtata tcgtaattta 65820 atctcctatt attggacaac tacattgttt ctaaaattat actattccta tgactaaacc 65880 tttgcatata tcttttatct ccctaggata tatttctaaa actagcattg ttgactgaaa 65940 gtgtaaatac gtgttaaggt gtttgctaca taatgccata tttccttttt aggaaactaa 66000 gctactttgg atttccacca acactgtatt catgtaccca tttttctctt aacctaactt 66060 tattggtctt tttaattctt aacagagacc agaactttgt aattcaacat tcatcgttgt 66120 gtaaattaaa cttctcccat tcctttcaga gggaacccct tacctggaat ctggaatcag 66180 cctcttctct gatgaccctg aatctgatcc ttctgaagac agagccccag agtcagctcg 66240 tgttggcaac ataccatctt caacctctgc attgaaagtt ccccaattga aagttgcaga 66300 atctgcccag agtccagctg ctgctcatac tactgatact gctgggtata atgcaatgga 66360 agaaagtgtg agcagggaga agccagaatt gacagcttca acagaaaggg tcaacaaaag 66420 aatgtccatg gtggtgtctg gcctgacccc agaagaattt gtgagtgtat ccatatgtat 66480 ctccctaatg actaagactt aacaacattc tggaaagagt tttatgtagg tattgtcaat 66540 taataaccta gaggaagaaa tctagaaaac aatcacagtt ctgtgtaatt taatttcgat 66600 tactaatttc tgaaaattta gatctagata aagctatagt gtggattatt ttatgtatat 66660 ttacttgaga aaataattat taaatattag tggaaaagct atactttggg tatgatatag 66720 gactttcgaa ttggaatttt cctttctatc tgtaaaagca agtaggtata gttttattcc 66780 ccagaaggca tctttttctc ccccttgtct cacatgggtg aatttaccag catatttaac 66840 taaattcaga ctggttccaa atgtactgcc agatagtagc atttctctag tgtttgtttt 66900 catcctggct tgtaagaatg ccctgccact tctgccctgc aatatccctt gctattagga 66960 ttttggcatc accttgggtc cttaatgcca gaaatgggaa ttgcttcata ctgtggaaaa 67020 atacccatta aaatattaag accagtaaaa cctcgtttct gcttgggcta tttgtggatt 67080 tcagacatcc tgagaagttt accacccctg taattaattg tcattgtcat cacttcataa 67140 taaaaataat tgcatggccg ggcatggtgg ctcaagcctg taatcccagc actttgggag 67200 gctgaggtgg tcagatcacc taaggtcagg agatcaagac cagcctgacc aacatgaaga 67260 aaccccatct ttactaaaaa tacacaatta gccgggcgtg gtggcgcatg cctataatcc 67320 cagctactca ggaggctgag gcaggagaat tgcttgaacc cgggaggcgg aggttgcggt 67380 gagccgagat tgcaccattg cactccagcc tgggcaacaa gagcgaaact ctgtctcaat 67440 aataagaaga agaattgcgt gaatatttct ttaaaactat gatgagataa cataccagat 67500 tatcaaatgg attcagtagt gggtgtgcca tttattgcac actgagagat gaccaagtca 67560 ttctgaaata tctttattaa tatatccttc ctaggatttt tcatcctaac ttctccatag 67620 gtagttactt agcataacat ctctgtggcc agatgtatcc cactactaaa agggcaaagt 67680 aagctgtggc tgccctggta gatacaatga gtaagtgcac agtgatggct ataaatgttt 67740 tcatctcata atcccatgtc cagaccagca atttgctctg aaagctctta cctgtgtctg 67800 tttcaatggc tcttgatcac ttgcctgcac gtccagaatt ccttatttat tcattgaaaa 67860 ttagcgttct ttatcccttt gttttgcaag ttcagctttt tagagatggc taaaatggtc 67920 taatctttct tggcaaaggc aattctgagc tgcagattag actacaagtg gcttgggtac 67980 atgttgtctt taaacaagcg aagaggaaaa ctttgagctc tattcagact tggtgaagtg 68040 tggtaaattt atgatgaaag ctactgactg tattacacat gattaattct gaagcccata 68100 ttaagatgat cttttcagca gttcagcatt gctcttctaa ctgaacagtt tcaaggctgg 68160 gatttcagca attaatcagt tcagaattgc taatgatctg gcggagggtg gtagcaaaag 68220 ggggaggatg tcattagctt ctctagcctg ccttttttca gtgccctgtg gcagtatgga 68280 gtgaggcaac atgaaagaaa gatggcctga ccttcatggc agtattgtgc aacacgtaaa 68340 tactggtgtg agtggctgtg gctatggcta gtaaatgatg gcccttggta aacaaagtta 68400 tttatcagac aatacctacc agctaggtca actgtgccca taattgatct ggttaatttc 68460 ttttgctgcc tattgatttt tatttggttg atagataata gctagaggac tctaaatttc 68520 tttggggaag aacatgaacc ccttctaagc cttcttacga gagaattgat cgcttttgca 68580 ctgaccttta gtaacatcct gatttcagtg ttttgtaact atcagagggt tgagtcttgg 68640 ttttaagcca tgtatatctg tagcataact ttctgtgtag gctagttacc tctcagctta 68700 taaagtgtag gctgataaat ttatagtaca gtagagtgtc actatgcaaa gaaacgatct 68760 tagggaatcg aatgatatct gctattaaag caaaattaat atatattttt tctttttact 68820 tttttttttt tttaaagaca tgaaatctca ctgtattgcc caggctggtc ttggtctcag 68880 actcttgagc tcaagcagtc ctcccacctc agcttcccaa agtgctggga ttataggcat 68940 gagctgccgt gtctggccca gtatatattt tttaagtttt aagttttgtg gtacgtagta 69000 ggtttataat attattttga atccttagtt gtaattttat gtctgctgat gtgtacataa 69060 tttttattaa actatttatt tgagacttca ggtatctttt tttttttttt gagacggagt 69120 ctcgcactct cgcccaggct agagtgcagt ggcgccatct cggcttactg caagctctgc 69180 ttcctgggtt cacgccattc tcctgcctca gcctcctgag tagctgagac tacaggtgcc 69240 cgccaccacg cctggctaat tttttgtatt tttagtagag acagggtttc accgtgttag 69300 ccaggatggt ctcgatctcc tgaccttgtg atctgcccgc ctcagcctcc caaagtgctg 69360 agattacagg cgtgagccac cgcgcccagc cgagacttca ggtgtcttag aattttttaa 69420 atgtaccctt tctgagaaaa acagagactt aaagctagga taactggtat tctatttttt 69480 tttttttttt ttttttttac ctccagcctg ggtgacagag caagactctg tctaaaaaaa 69540 aaaaaaaaaa aattcacttt aaatagttcc aggacacgtg tagaacgtgc aggattgcta 69600 cataggtaaa catatgccat ggtggaataa ctagtattct gagctgtgtg ctagaggtaa 69660 ctcatgataa tggaatattt gatttaattt cagatgctcg tgtacaagtt tgccagaaaa 69720 caccacatca ctttaactaa tctaattact gaagagacta ctcatgttgt tatgaaaaca 69780 ggtataccaa gaacctttac agaatacctt gcatctgctg cataaaacca catgaggcga 69840 ggcacggtgg cgcatgcctg taatcgcagc actttgggag gccgaggcgg gcagatcacg 69900 agattaggag atcgagacca tcctggccag catggtgaaa ccccgtctct actaaaaaat 69960 aaaaaaatta gctgggtgtg gtcgcgtgcg cctgtagtcc cagctactcg tgaggctgag 70020 gcaggagaat cacttgaacc ggggagatgg aggttgcagt gagccgagat catgccactg 70080 cattccagcc tggcgacaga gcaaggctcc gtctcaaaaa aaaaaaaaaa aaacgtgaaa 70140 aaataagaat atttgttgag catagcatgg atgatagtct tctaatagtc aatcaattac 70200 tttatgaaag acaaataata gttttgctgc ttccttacct ccttttgttt tgggttaaga 70260 tttggagtgt gggccaggca cggtggctca cacctgtaat ctcagcactt tgggaggccg 70320 aggcgggtgg atcacctgag gtcaggagtt cgagaccagc ctggccaacg tgttgaaacc 70380 ccgtctctac taaaaatata aaaattaggt gggcgtggtg gcaggcacct gtaatcccag 70440 ctactcagga ggctgaggca gcagaatcgc ttgaacccag gaggtggagg ttgcagtgac 70500 ccaagatcgc accattgcac tccagcctgg ggacaagagc gagattcttg tctcaaaaaa 70560 aaaaaaaaaa aaaaaaggtt tggagggtgg tgagctgaga tagtcaacta ttaactccta 70620 tctacctgct gggactacac tggtgaggtg gagcctaagt cctaaaacaa caagtgaggc 70680 agctggacgc ggtggctcgc atcagtaatc ccagcacttt gggagcctga ggcgggcaga 70740 tcacaaggtc aggagttcga gaccagcctg gccaatatgg taaaacccag tctctactaa 70800 aaatacataa attggctggg cgtggtggtg tgcacctgta atcccagcta cttgggaggc 70860 tgacacagaa gaattgcttg aactctggag gctgaggttg cagtcagctg agatcctgcc 70920 actgcactcc agcctggcga cagagtgaga ctctgtctca acaacaacaa aagaaagaac 70980 aagtgaggca aaacctggag accccagctt catgtaacac ctagtttgag tattgttgag 71040 agtttttcag gaaaaaagtc tgataacagc tccgagatag tcttaacata tgaaaaagca 71100 aaaaagggag gagacagatc atttgtccta tacctttctc ttttaaggtt ttaattataa 71160 cttgtgtaat acaggagacc tctgggtgtt tttagttgac tataaactaa atctgagtac 71220 acatttcagg gctgctaaaa atgcttattt gaaactgggc cgtattaaca caagcagagg 71280 ctctggagca agtgaagtac agatccagag ccccactgta ttctccaatg gagtgattgc 71340 ctgaaagatg atgtcagttt taagcaccgt gcttggtttt taacatggtc actgacaaat 71400 tggagagtgt ttatccagag gtagatggta aagatacata aaagtaactt gaaatactgt 71460 cttttgaaga agaaatgaga agatttaagg aaataagaca ctgtcttcaa gtatctgaag 71520 aaccgttacc cggaagagaa ctgttatctg gaacaggatt aagactcact catggggctc 71580 cagaaagcag acgagtgcat ggaggacgca gaagatgcag attgtgtggc tcaactctaa 71640 aatctttcta acaaaattag ttctctggat gtgttccagt tcacttgatg atgattcttt 71700 tgtttttgtt tttgtttttg aggtgtagtt tttcactctt gttgcccagg ctgctggagt 71760 gcaatggcac gatcttggct tgctgcaacc tccccctccc gggttcaagc gattctcctg 71820 cctcagcctc ccgagtagct gggattacag gaatgcacca ccatacctaa ttttgtattt 71880 ttagtagaga cagggttttt ccatgtcagt caggctggtc ttggactccc gacctcaggt 71940 gatccaccta cctcggcctc ccaaagtgct gggattacag gtgtgagcca tcgcgcctag 72000 cctatgatga ttcttttcac agagatacag gcacttaagg agaggatcta aaccccttgg 72060 acacattgcc gttgaacttc taagatctta ggtttccact tactcatgaa aattatacca 72120 cagggtcaga gggtagtgtt cattggagcc aggtgccaga acaagttatt acaaactact 72180 attttagaga aaaatgtcat taaagtttaa gataccttaa gctataggtt tgcatcaaag 72240 ttaatgaaag gtaaaaagat gccaagcgtg gtggctcagg cctgtaatcc cagcgctttg 72300 gggggccaag gcgggcagat cacgaggtca ggagatcgag accatcctgg ctaacacggt 72360 gaaaccccat ctctagtaaa aatacaaaaa attagccggg catggtggcg ggcatctgta 72420 gtcccagcta ctcaggaggc tgaggcagga gaatggcatg aacccaggag gcagagcttg 72480 ccgtgagctg agatccagcc actgcactcc agcctggctg acagagcaag actgcatctc 72540 aaaaaaaaaa aaaaaaaaaa atgcaaatca aatctaaagt agttcagtct ttaaactcaa 72600 agccaataca tttgctttga actacaaatg aactgaagtt tttaagtgta ataaatgtta 72660 ctaaatcggc ttttgtagca gttaaacaaa aaacttcaaa aattgtaagg attctgtgag 72720 ggagcatggc tgctgctgct gctgctgctt gcagatagcc tgctgtgttt aggatttagt 72780 taaatacatt tctcctgttt aaaactaaat ggtctttcct tagtttgctt agttcttcag 72840 aagggccttt gaaacactgg gaaataaaca agtgattctt tagctactgc tttctgaaat 72900 acttatataa aagctctgca ctgtattctc ccatccctct caggggaata ttagagggtt 72960 aggactcccc aggtagacat tctaggggtg aaaatttgtc attacattga catttcagat 73020 ttaggttttc aacaatactg ttttcttctt tcacatattg ccatctagta atatagatgt 73080 tctccgtcca cattaatcaa aactattgac atggataatt cctaattcct tgaacactat 73140 aatggagatc tatagctagc cttggcgtct agaagatggg tgttgagaag agggagtgga 73200 cagatatttc ctctggtctt aacttcatat cagcctcccc tagacttcca aatatccata 73260 cctgctggtt ataattagtg gtgttttcag cctctgattc tgtcaccagg ggttttagaa 73320 tcataaatcc agattgatct tgggagtgta aaaaactgag gctctttagc ttcttaggac 73380 agcacttcct gattttgttt tcaacttcta atcctttgag tgtttttcat tctgcagatg 73440 ctgagtttgt gtgtgaacgg acactgaaat attttctagg aattgcggga ggaaaatggg 73500 tagttagcta tttctgtaag tataatacta tttctcccct cctcccttta acacctcaga 73560 attgcatttt tacacctaac gtttaacacc taaggttttt gctgatgctg agtctgagtt 73620 accaaaaggt ctttaattgt aatactaaac tacttttatc tttaatatca ctttgttcag 73680 ataagctggt gatgctggga aaatgggtct cttttataac taataggacc taatctgctc 73740 ctagcaatgt tagcatatga gctagggatt tatttaatag tcggcaggaa tccatgtgca 73800 gcaggcaaac ttataatgtt taaattaaac atcaactctg tctccagaag gaaactgctg 73860 ctacaagcct tattaaaggg ctgtggcttt agagggaagg acctctcctc tgtcattctt 73920 cctgtgctct tttgtgaatc gctgacctct ctatctccgt gaaaagagca cgttcttctg 73980 ctgtatgtaa cctgtctttt ctatgatctc tttaggggtg acccagtcta ttaaagaaag 74040 aaaaatgctg aatgaggtaa gtacttgatg ttacaaacta accagagata ttcattcagt 74100 catatagtta aaaatgtatt tgcttccttc catcaatgca ccactttcct taacaatgca 74160 caaattttcc atgataatga ggatcatcaa gaattatgca ggcctgcact gtggctcata 74220 cctataatcc cagcgctttg ggaggctgag gcgcttggat cacctgatgt cgggagttca 74280 agaccagcct gaccaacatg gagaaacccc gtttctacta aaaatacaaa attagccggg 74340 cttggtggca cttgcctgta attccagcta ctcgggaggc tgaggcagga gaatcacttg 74400 aacctgggag gcgggggttg cagtgagctg agatcgcatc attgcactct aacctgggca 74460 acaagagcaa aactccatca aaagaaaaaa aaaatcgggt gcagtggctc atgcctgtaa 74520 tcctaacact gtgggaggcc aagacaggca gattgcctga gctcaggagt tcgagatcag 74580 cctgggcaac atggtgaaac cctgtctcta ctaaaataca aaaaattact cagcgtggtg 74640 gcatgcgcct ttagttccag ctactcagga ggctgaggca ggagaatctc ttgaacccgg 74700 gaggtggagg ttgcaatgag ccaagatcgt gccactgcac tccaacctgg caacagagcg 74760 agactccgtc ttaaaaaaaa aaaaaatttt gcagcgcaaa ccaggatatc ctctgttctc 74820 atttgttcta gatttcaaaa gaaacagtcc tttctttggg gaaaagagaa aggaaaagga 74880 gttttataaa aggaaagaaa agattcataa gaacaagaag tgggcccact tgcatatacc 74940 tttgtagaaa actgttcact gttgttgaag aaaagctctt catattaata tgcagtccag 75000 atgcagtggc tcacacttat aatctcagcc ctttgggagg ctgagacagg aagattactt 75060 gaggccagga gtttgaaacc agcctgggca acatagtgag actctgtctc cacaaaattt 75120 ttttttaatt agccgggcat ggcagtgtgc ttctgtagtc ttagctactg aggaagctaa 75180 gccagaagaa tcacttgagc ccaggagttc aaggctgcag tgagctatga tcataccatt 75240 gcactcttgc acttgcacag agcaagaccc tgtctcttaa aaaaaaaaaa gtgtgtgtgt 75300 gcatatgcat atatacatat atatacatgc aaatgtatct gtttataatt cagattgctt 75360 caaaaagatg ttgcacttta tgatactgag aacagtgaga agtaaataag atagagtgta 75420 ggaggaggaa taatttcaga acagccatct gagaacttct gtgacaacag atcaggcaaa 75480 atgaaatgtg aaagtaattt tataggccag gcgtggtggc tcatgcctat aatcccagca 75540 ctttgagtgg ccaaggcagg tggatcactt gaggtcagga gttcgagacc agcctggtca 75600 acatggtgaa accttgtctc tactaaaaac acaaaaaaat tagtcgagcg tggtggcatg 75660 tgcctgtaat cctagctgct ggggaggctg aggcaggaga atcacttgaa cccgggaggc 75720 ggaggttgca gtgagcctag attgcaccac tgcactccag cctgtgagac agaatgagac 75780 cctgtcttaa aaaaaaaaaa aaagtaattt tataaactat tgtgcacaat tcgatgtatt 75840 cataattaat taaatgatta tttttgttgg ttttaacttt tattcagtgg ctatttattg 75900 ggagcctact gtgttctggg cactaggaat gcaacagtaa ataagactaa ctaagtccct 75960 ggtaggattc aggttctgtc gaggggagat acacaataaa gatgaattta agataacaat 76020 aaatgctatg gagaaatata cagaacagtg gaatagtatt agctgtcaaa ggttgttgat 76080 tactttcgtt taaggaggcc agggaaagcc tttctgaaaa aattgagctg agacctaaat 76140 aacaagaaat aattgtcctt gaaaaatgaa gggaatgcat cttataggca gaggaatagc 76200 aaacataaag gtcttgaggt aataatgagt gtggtttttt gatttctgta ttttggtttt 76260 tttgagatgg tgtctccctc tatcccccag gctggagtgc agtggcacaa tcttggctca 76320 ctgcaaactc tgtctcctgg gttcaagcaa ttctcctgcc ttggcctcct gagtagctgg 76380 tattacaggc acgcgtgcta ccacacccga ctagttttta tttttagtag agatggggtt 76440 ttaccacgtt ggtcaggctg gtctcaaact cctgaactca agtgatccaa ccacctcaac 76500 ctcccaaagt gctgggatca caggcgtgag ccaccatgcc cggccagagc ttggtttatt 76560 ttttaaaaga taggccaatg ttggtcgtgt gtggtggctc gtgcctataa tcccagcact 76620 ttgggaagcc aaggcaggca aatcacttga ggtcaggagt tcgagaccag cctggccaac 76680 atggtgaaac cccatctcta ctaaaaatac aaaaaactag catggtgtgg tggtgtgtgc 76740 ctgtaatccc agtgcctgta atcccagcta ctccagaggc tgaggcagga gaatcacttg 76800 aaccgaaagg taggagttac agtgagccaa gatcgcatca ctgcactcca gcctgaacga 76860 cagagcaaga ctcctgtctc aagaaataat aatgataaaa ggttcgggca cagtggctca 76920 cacctgtaat tccagcactc taggaggccg aggcaggcag atcccctgag gtcaggagtt 76980 tgagaccagc ctggccaacg tggcaaaacc ccatctctac taaaaaatgc aaaaattagc 77040 tgggcacggc tgggtgtggt ggctcattcc tgtaatccca gcactttggg aggtcaaggc 77100 ggacagatca ctgaggtaga aaccctgtct ctactaaaaa tacaaaaatt tgcccagcgt 77160 ggtggcgcgt gcctctaatc ccagctacac gggaggctga gacaagagaa tcacttcatc 77220 aacccgggag gtggaggttg tggtgagctg agatcgcacc attgcactcc agcctgggca 77280 acaagagtga aactccatct caaaaacaaa aaaaaattag ctgggaatgg tggcatgtgc 77340 ctgtaatcac agctacttgg gaggctgggg caggagaatc gcttgaaccc aggaggcgga 77400 gattgcagtg agctgagatt gcgccactgc actccaggct gggcgaaaga gcaagactcc 77460 gtctcaaaaa taataataat aataataata ggccagtgta gctggagtaa tttgcaaatt 77520 atgtgtggag gcagagatta cacaaggaat gggagaaggt catagatgag ggccagatca 77580 catagtattt ggtggtaagg aattcagatt ttatccttgt ggtaattggt ggtgtggaga 77640 tggttaaaaa caaggttggt ttgggatggg tttgaagaga ggacttgcta atggattaaa 77700 tttggaggat aaggtaaaga gaaattgaag gagtgacact tgggttttgg cttgaacaat 77760 agatcttgtt agtaatatta aattagatga agaaggcatg gtagggaata tgggggagtg 77820 ggaaaggcag gaagcaggaa tggaaccagg aactctgttt tagatgtgag aatttgttgt 77880 tgttgttgtt gttgttgttg ttgttgttgt tgttgttgtg acagcatctc gttctgttgc 77940 ccaggctaga gtgcatggag tgcggtagca cgatctcagc tcactccaac ctccgcctcc 78000 cggttcaagt gattttcctg cctcagcctc ccgagtagct gggattacag gcacctgcca 78060 caatgcctgg ctaatacttg tatttttagt agagatgggg ttttaccatg ttggccaggc 78120 tggtcttaaa ctcctgacct caggtaatcc acccacctcg gcctcccaaa gtgctgggat 78180 tgcaggtgtg agccactgtg cccggccaga tgcatgaatt ttgagatgta tactagactt 78240 ctggatagag aagttaagta ggcagttgga cacattgtat gaagctcagg ggtacaagga 78300 ggactatgaa catgggagtc ttctgacaaa tttatcacta gactcctcat tcaagtaact 78360 aggaaatgtc agatattctt cccctagtaa tagccagtgg ttatactctt gcctttagtt 78420 ttcttcacaa tactcttggc aacacataag gccttcccta caatctgagt ttcagtcaga 78480 attgtttctg agcgttcttc ctcaaatttc tccccagtct cattattctt tattctcatg 78540 tccatgacca gtcataatag taattatgaa aaacctctaa ctttctttag tgcattgaat 78600 gtatatttta tcattttggt tgtgttaact gtaaatctct cagtggaaat ctgaaaagcc 78660 tttatttcct tagatgataa tatacaattg atttaggaga tagggaattt ttcagttacc 78720 tttataacag cacagtatta gcagtctaat ctaaatgcta agtgaatgtt ttgagaggag 78780 atagatgttg aaaattaaaa tacattaagt cccagtgagg tgaaaagccg attgttaagt 78840 tctgcacaca aaagatttgc ttcagtgaat tgatttcaac agctgagatc ctagtcattt 78900 cacctggtct accaaaaaga atgattttac ttgcttttgg tcaaatctct gcccagcaat 78960 tctttttctt tctttctttt ttttgtttta tgtgtgtgtg tgtgtgtgtt tttttttagc 79020 agagtctcac tttgtcaccc aggcgggagt gtggtggtat gatcacagtt cactgcagcc 79080 tccaactcct gggctcaagt gatcctccag cttcagcttt tcaagaaatt gggactgcag 79140 gcacatgcaa ctatgcctgg ctgaggtttt atgtatcttt tttctagaga aggggtctca 79200 ctgtgttgcc cagctgggtc tccagctcct ggtctcaagc tgtcctcctg cctcagcctc 79260 ccaaagtgcc aaagtgctag ggttataggt gtgagccatt ggtgcccagc tactgcctgc 79320 ctggcaattc tgaatgcctt aaattttttt tttttttttt tttttttttg agacagagtt 79380 tcactctgtc acccaggctg gagtgcagtg gcatgatcgt ggctcacagc aacctctgcc 79440 tcctggattc cagcaattct catgcctcag cttcccgagt agctgggact acaggtgcat 79500 gccaccacgc ccagctaatt tttggttttt ttgtttgttt gtttgtttgt tttgagacgg 79560 agtctcgctc agttgcccag gctggagtgc agtggcgtga tctccgctca ctgcaagctc 79620 cgcctcccgg gttcacgcca ttctcctgcc tcagcctccc gagtagctgg gactacaggc 79680 gcctgccact acacccggct aatttttttg tattttaagt agagacgggg tttcaccgtg 79740 ttagccagga tggtctcgat ctcctgacct cgtgatccgc ctgtctcggc ctcccaaagt 79800 cctgggatta caggcgtgag ccaccacacc cggcctaatt tttttttttt taattttatt 79860 tttaattttt tgagatgcga gatggagtct cgctctgtta cccaggctgg agtgcagtgg 79920 caccatctca gctcactgca acctccacct cctgcattca aaagattctc ctgcctcagc 79980 ctcccaagta gctgggatta caggtgcctg ccaccacgcc caactaattt tttgtatttt 80040 tagtagagat gaggtttcac catgttggtc agactggtgt cgaactcctg acctcaagtg 80100 atctgcctgc ctcagtctcc caaagtgcta ggattacagg ggtgagccac tgcgcctggc 80160 ctgaatgcct taaatatgac gtgtctgctc cacttccatt gaaggaagct tctctttctc 80220 ttatcctgat gggttgtgtt tggtttcttt cagcatgatt ttgaagtcag aggagatgtg 80280 gtcaatggaa gaaaccacca aggtccaaag cgagcaagag aatcccagga cagaaaggta 80340 aagctccctc cctcaagttg acaaaaatct caccccacca ctctgtattc cactcccctt 80400 tgcagagatg ggccgcttca ttttgtaaga cttattacat acatacacag tgctagatac 80460 tttcacacag gttctttttt cactcttcca tcccaaccac ataaataagt attgtctcta 80520 ctttatgaat gataaaacta agagatttag agaggctgtg taatttggat tcccgtctcg 80580 ggttcagatc ttagctgata agtggaagag ctgggacttt aagcagatga gaatctaaag 80640 actttgctct tttcacttca ctggggtgtc tttctctctc tctctcttgc tctctctctc 80700 tctttttttt tttcccaaga cggagtctca ctccattgcc caggccagag tgcagtggtg 80760 cgatctcagc tcactgaaaa ctcatcttgc ccaggctggt cttgaacccc tgaccttgtg 80820 atcctcccgc cttggcctcc ccaagtgctg ggataggcgt gagccaccgt gcccagccaa 80880 taatagctaa aatttatata atgttcactg ggccaggcac agcggctcgt tcctgttatc 80940 ccagcacttt gggaagctga ggcaggcaga tcgcttgagc caaggagttc gataccagcc 81000 tgggcaacat ggcaaaaccc catctctacc aaaaaaaata tacaaaaatt agccaggcgt 81060 ggtggcatgt acttgtagtt ccagctactc ggaaggctga gttgagagta tctcttgagc 81120 ccaagaagag gggactacag tgaacggaga ttgcgccact gcactccagc ctagacgaca 81180 gacagaagat ctcaaaagaa aaaaaaaaaa aaaagatcac tttatgctgg gactgctcta 81240 aaggcccaac catgttttaa ctaattaaca attttatgac aactctatga gctatgtact 81300 gtaattatgc ctatattaca gatgtgaaaa ttgaggctca gagaggttga ataagttgct 81360 caaagtcaca caggtaataa gtgatggaac tagaagttga actcaggaag tctagctcca 81420 agtctaaatt ctttgttaat ttatttttcg ggccagagtc ttactctgtc acccaggctg 81480 gagtgcagtg ccactatctc tgctcactgc aaccttcacc tcccaagttc aaaccttgtt 81540 caattcttgt gccttggcct cccaagtggc taggattaca ggcatgtgcc acaacaacta 81600 gctaattttt tgtctgattc tgttggccag tctggagtgc agtggcgcaa tctcagctca 81660 ctgcagtctc cagctcccag gttcaagtga ttctcgtgcc ttagcctccc aaatagctgg 81720 gattacaggc acgtgccacc acaccgagat agttttttgt atttttaata gaaacaaggt 81780 ttcaacatgt tggccaggct ggtctcaaat tccagacctc agatcatctg cccgcctcag 81840 gctcccaaag tgctgggatt acaggcatga gccactgcac ccggccttaa tttttatatt 81900 tttattagag atggggtttt gccatgttgg ccaggctggc cttgatctcc tggcctccag 81960 tgatccaccc gccttggctt cccaaagtgc tgggattaca agcatgagcc actgcacccg 82020 gcctccaatt ctaaactctt aacaacaata ctatagtttc ttgaaaagtt gttgaaggct 82080 tcacggaggg aaaaaaaatg gagcattcta acaactttgc agatgagacc caagaagact 82140 caatgacttt ctcctgatca tattgtagca gatgacttag ccagaactct gacttcctca 82200 cagggagaaa gtctgcaaga tttcacactt acctgtcagg cctgagctgg ctgctttctc 82260 agctccctaa gtgctatgtt cccagtctgc ttttcttcct ttttcaagtg tgcactacca 82320 ggcatttcag aacatcccag gctggtcgcg gtggctcaca cctgtgatcc cagcactttg 82380 ggagcccaag gcgggtggat cacctgaggt caggagttcg agaccagcct ggccaacatg 82440 gtgaaacccc atctctacta aaaatacaaa agttaactgg gcgtggtggt aggcacctgt 82500 aatcctagct caggattact cgggaggctg aggctagaga atcggttgaa cccaggaggc 82560 ggaggttgca gtgagccaag attgcgccac tgcactctag cctggggaca agagggagac 82620 ttcatctcaa aaaaaaaaaa aaaatcccag ctgggcacag cggctcactt ctgtaatccc 82680 agcactttag gaggccaagg caggaggatc acttgagccc aggagttcaa gactagcctg 82740 ggcaacatag taagaccctg tctctacaaa aaaatttaaa aattaattgg gtgtcgtagc 82800 acactcttgt attcccagct actcaggagg ctgaggtgag aagaatgctt gagtctggga 82860 ggtcgaggct gcagtgagcc atgatggtgc tactgcactc cagcctggcc aacattgtga 82920 gaccttgtct caaaacaaaa caaaacatcc ttctactgag cactttctgt ccctttatag 82980 aaacttaaga gggaaccagt agaggtaatt tcctaaggaa aactgctttg ggacatgatc 83040 acaaatgaag cctggagttt tgaactgctg aggtcagcct gtttttacct tctgagccta 83100 tcaagtaatt gttccagatg ccaagaaaag ctgctggcct tatttctgct tctgccttta 83160 ccacagggga gcgccatgtg agccagtcct ctgtttttcc tccactgtat gctaggcagt 83220 attagcacca gattcttccc ctctttaaaa agaaattcta gtgctttgga ttttttcctc 83280 catgcagaat agcaatgatg gaaagtatgt ggtcaaagta atgacattct gaaaatacta 83340 aatgtcacca tagtattttt ctctggaaga gaaatgtata tgtagaggtg aaacttcaaa 83400 tttctttttt ttttttttta agacgaagct ttgctcttct tgcccaggct gaagtacaat 83460 ggcgtgatct tggctcaccg caatctctgc ctccagggtt caagtgattc tcctgcctca 83520 gcctcctaag tagctaggat tacaggcatg tgccaccacg cccagctgat tttgtatttt 83580 tagtagagat ggggtttctc catgttggtc acgctggtct tgaactcccg accccaagtg 83640 atccacccac ctcggcctcc caaagtgcta ggattacagg ccaccgcgcc cggcctgaaa 83700 cttcaaattt cttttttttt ttgagacaga gtctcgctat gtcacccagg ctggagtgca 83760 gtggcgccgt ctcggctcac taccagctcc actccacctc ctgggttcac accattctcc 83820 tgcctcagcc tcccaagtag ctgggactac aggtgcccgc caccatgccc agctaatttt 83880 ttgtattttt agtagagacg ggttttcact gtgttagacg ggatggtctc catctcttga 83940 cctcgtgatc cgcctgcctc agcctcccaa agtgctggga ttacaggcgt gagccactac 84000 gccaagcccg aaacttcaaa tttcttatct cataactagg catccttatc actgagtgtt 84060 agcctggata taaacattcc taatcttttg tacttttcat gtcagcattt ggctccactt 84120 ggctgcctgg ggagaacttc tagcattatg agcatgcagg tcctatcaac aggttggggg 84180 tgcggtttat tcatacaggt agtgagagtg gcacagatgg atgctgtccc ttaaaacaaa 84240 cagacttgtc tttgggagcc tgaggcgggt ggatcatgag gtcaggagtt caagaccagc 84300 ctggccaaca tagtgaaacc ccgtttctac taaaaataca aaaaattagc cgggtgtggt 84360 ggtgtgcacc tgtaatccca gctactaggg aggctgaggc aggagaatca cttgaaccca 84420 ggaggtggag gttgcagtga gccgagatgg caccattgca ctccagccca ggcgacagtg 84480 caagactgcg tctcaaaaaa aaaaaaaaaa cacacagact tgtcctactg ccatttcttt 84540 tcactctggc ggtaaagtaa gagtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt 84600 gtgtgtgtgt gtttctgtcc gtctgtctgt caagggggag ggtgaccact ttctaaaagg 84660 ccatccgtgt atttttagct tcctgatttt tttctctatc gcagtctctt tgaagccagg 84720 tgaattttag gccttggcaa ttttcttttt attgcaatgg gaaggtcaag acactgagag 84780 tcacccaaaa catatccatc caaaatgata caattttagg gtttattttt aagtgatacc 84840 caagttattt gctaagaacc tatgccagtg tgtttatgag aatttgcact gtcccacact 84900 gttgccacca gccacatggg actgtttaaa tttaaatttt acaaattagc cagtcatggt 84960 ggtgtgcact tgtagtccca gctacttagg aggctgaggc aagaggattg cttgagccca 85020 gaagttcaat actgcagcaa gctatgatcg tgccactgta ctccagcctg agtgacagaa 85080 tgagacctca tctcttcaaa aaaaaagaaa aaaattaaaa tatgaagttt agttcttcat 85140 tcaccctaac cacatctcca gtgctcaata actatatgtg actcatggct accttattag 85200 catagatata gaacattgtg actatcacag aaagttgttt tgaacagtgt tgccaagccc 85260 tgtaagtgga agaggcagtg cagtgtgatc tgtgtcttca ggaaaccagg tagtcagact 85320 agttcaatga ggagaggcag aacctggctt cacttctaga ttaaaaactg cttaggtggc 85380 ctaaagatac aatggccatt ctcagagtag tgagaaggaa ggaacagatg tttagggggc 85440 tagaagaaag tcagagaggg ccgggcgcag tggcttatgc ctgtaatccc agcactttgg 85500 aaggccaaga caggcagatc acgaggtcag gagttcgaga ccagcctgac caacatggtg 85560 aaaccctgtc tctactaaaa atacaaaaat tagccgggcg tggtggtgcg cgcctgtaat 85620 cccagctact caggaggcta aggcaggaga atcgcttgaa ccctggaggc agaggttgca 85680 gtgagcccag atcgcaccac tacgctccag cctaggtgac agagagagac tccgtctcaa 85740 aaaaaaaaaa aaaagtcaga ggagacaagg agcatgtaca cctaaaatca acatagaccc 85800 ctctgttgat ggggtcatag tgagtacttg aggtaccaag tctggataaa catcaaactt 85860 cagccaataa ctttgagttt ctagccatcc aagcctctta ttaaacatac agaaggacct 85920 tttttccctt gcatctaaca agttaaagca cctgcagaga tcattaggga ggagccttgg 85980 cctgattggt gacaaaagtg agatgctcag tccttgaatg acaaagaatg cctgtagagt 86040 gcaggtcaac tacatatgca cttcaagaag atcttctgaa atccagtagt gttctggaca 86100 ttggactgct tgtccctggg aagtagcagc agaaatcatc aggtggtgaa cagaagaaaa 86160 agaaaagctc ttcctttttg aaagtctgtt ttttgaataa aagccaatat tcttttataa 86220 ctagattttc cttctctcca ttcccctgtc cctctctctt cctctcttct tccagatctt 86280 cagggggcta gaaatctgtt gctatgggcc cttcaccaac atgcccacag gtaagagcct 86340 gggagaaccc cagagttcca gcaccagcct ttgtcttaca tagtggagta ttataagcaa 86400 gatcccacga tgggggttcc tcagattgct gaaatgttct agaggctatt ctatttctct 86460 accactctcc aaacaaaaca gcacctaaat gttatcctat ggcaaaaaaa aactatacct 86520 tgtccccctt ctcaagagca tgaaggtggt taatagttag gattcagtat gttatgtgtt 86580 cagatggcgt tgagctgctg ttagtgccaa catgttagtg agaaaatatc tttggatagg 86640 taaaaatcaa ggaggagttc tcctcttcct aaaccatctt aatttactta catagaagaa 86700 agcacagcag ctggcccacc acggacgggc ccagagcagg ggaagattct cggtgaacat 86760 ttcttttttt ttttcttttt ttttgaggtc gagtctctgt tgcccaggcc agagtgcaat 86820 ggcgcgatct cggctcactg caacctccac ctcccgggtt caagtgattc tcctgcctca 86880 gcctcccaaa tagctgagac tacaggcgtg tgccaccacg cccgactaat tttttgtatt 86940 ttttttttag tagagacggg gtttcaccgt gttagccaat atggtcccga tctcctgacc 87000 tcgtgatcca cccgcctcag cctcccaaag tgctaggatt acaggcatga gccactgtgc 87060 ccagccctct ccatgaacat tttctaatta aacttgacac ttaatacaat gttatgctta 87120 ggactgctat aaagcttacc tctggagttg cgcagcacaa aggccttggt gtgtgtataa 87180 atttggtttg ttcttttcac agcaaaagct acccaccttt gcctcctgtg cctgcttctg 87240 cccagggact taggtcctct tacaccttag agaaaggcct tagcatctgg tcacaggcag 87300 atgagtgaca gcaagaaaac ctggctgcaa tgtaattttg tttccatcct ctttattagt 87360 tatcaattgg atttttatga aatttccaag ttccactcaa ggatttctca gtgttttttt 87420 actttggtat agtggaaacc agggttgcca gaaagtatta ttttgggggt gagttagtca 87480 accttcgttc agtcagacag acaggagcac ctcagcaatt cccagaaacg ggctgatggg 87540 aaagagcaac atacatgaat gtcttgaaga acacagccaa cagagcccat tgggcagttc 87600 tgattttcca ggtacacagc atctccacag tctcttctga tttttattcc cctgagtata 87660 tggattccag ctcagcatgt agcctttccc tgctgagtct ctaaccagga taacatgtat 87720 ttttttgact ggatgaatta tcttcccatc tcttgacatt tacagtaatt accaccaagt 87780 atggtatttt cagtggccgt gattatcagt taccaacaca gaattaggat gaagggagga 87840 agggagggaa ggaaggtggg tgttttttca cacagtgtct tagccagcaa tttagcaaat 87900 taatggaaat tagatctttg attttttttt ctttcaagca ttttatttga gagactatca 87960 aaccttatac caagtggcct tatggagact gataaccaga gtacatggca tatcagtggc 88020 aaattgactt aaaatccata cccctactat tttaagacca ttgtcctttg gagcagagag 88080 acagactctc ccattgagag gtcttgctat aagccttcat ccggagagtg tagggtagag 88140 ggcctgggtt aagtatgcag attactgcag tgattttaca tctaaatgtc cattttagat 88200 caactggaat ggatggtaca gctgtgtggt gcttctgtgg tgaaggagct ttcatcattc 88260 acccttggca cagtaagtat tgggtgccct gtcagagagg gaggacacaa tattctctcc 88320 tgtgagcaag actggcacct gtcagtccct atggatgccc ctactgtagc ctcagaagtc 88380 ttctctgccc acatacctgt gccaaaagac tccatctgta agggatgggt aaggatttga 88440 gaactgcaca tattaaatat actgagggaa gactttttcc ctctaactct ttttcccata 88500 tgtccctccc cctcctctct gtgactgccc cagcatactg tgtttcaaca aatcatcaag 88560 aaatgatggg ctggaggctg ggcatggtgg ctcatgtctg taatcccagc actttgggag 88620 gccgaggcag gtggatcact tgtcaggagt ttgagaccag cctggccaac atggtgaaac 88680 cccatctgta ctaaaaaaaa aaaaacaaaa agtagccagg cctggtggag catgcctgta 88740 atgccagcta tttgggaagt tgaggtgtga gcatcgcttg aacgtgggag gcagaggttg 88800 cagtgagcca agattgcacc actgcactcc agactgggtg acagagtgag actttgtcta 88860 aaaaaaaaaa aaaagagaga gagagaaaag ctaggtgcgg tggctcacgc ctgtaatccc 88920 agcactttgg gaggctgagg tgggcagatc acgaggtcaa gagatcgaga ccatcctggc 88980 caaccaacat ggcgaaaccc cgtctctact aaaaatacaa aaattagctg ggcgtagggg 89040 cgcacgcctg tagtcccagc tacttgaggg gctggggcag gagaatcgct tgaaccccgg 89100 aggcggaggt tgcagttagc caagatcgcg ccactgcact ccagcccggg cgacagagcg 89160 agactccgtc tcaaaaaaaa agagagagag agaaatgatg ggctgggcca gtgccccacc 89220 cctgtaatca caacactggg aggccaaggt gggagaatcg cttgagcctg ggagctgaag 89280 accagcctgg gcaatacagt aggacctcat gtctacaaaa aaattattaa aaattagcca 89340 aggctgggtg cggtggctca tgcctataat cccgggggtg aagttgagcc caggagtttg 89400 agaccagcct gggcaacatg gcaaaaccct gtctctacca aaaatacaaa aaaattagcc 89460 aggggtggtg gtacgtgtct gtagttccag ctacttagga ggctgagatg gaaggattgc 89520 ttgagcccag gaggcagagg tggcagtgag ctgagatcac accactgcac tccagcctgg 89580 gtgacagagc aagaccctgt ctcaaaaaca aacaaaaaaa atgatgaagt gacagttcca 89640 gtagtcctac tttgacactt tgaatgctct ttccttcctg gggatccagg gtgtccaccc 89700 aattgtggtt gtgcagccag atgcctggac agaggacaat ggcttccatg gtaaggtgcc 89760 tgcatgtacc tgtgctatat ggggtccttt tgcatgggtt tggtttatca ctcattacct 89820 ggtgcttgag tagcacagtt cttggcacat tttaaatatt tgttgaatga atggctaaaa 89880 tgtctttttg atgtttttat tgttatttgt tttatattgt aaaagtaata catgaactgt 89940 ttccatgggg tgggagtaag atatgaatgt tcatcacaaa aacataaatc aaggccgggc 90000 atggtggctc atgcctataa ttccagcact ttgggaggtc aagatggagg tcaaggtggg 90060 agcctagaag ttcgagacca gcctgggcaa cataaggaga cttcatctgt acaacaaatt 90120 taaaaagtag ctgggtgtgg tggcagatgc ctgtagtcgc agctacttgg gaagctgagg 90180 tgggaggatc acttgagctc aggaggttga tgcttcagtg agccacgatc acaccactgt 90240 actccagcct gggcgacaga gcgagaccgt gtctcaaaaa gaaaaaagaa agtataaatt 90300 tacacaaaaa caataaaata atcccagtaa ttccaccact tggagatgat caccataaaa 90360 ctccaccagg catatgtgcg tatatataca cgtgtatttt ataaaatgtg atcataatta 90420 cactgttttg cttttttcct taagatatta catacatttt tccacatcgt taaattacag 90480 tgctgttttc ctggtggctt tcctttaaca gattgaagtt catgttaata cagttgccag 90540 aggctgtggg ctttcactgt caccaggagt cactcctagg gcctcttcag agcaaggcct 90600 tatgtcctga agcattgcct tttttttttt tttttgaggt ggagtctcac tctgtcactt 90660 agcaggctgg agtgcagtgg cccagtcttg gctcactgca acctccgcct cctgggttta 90720 aatgattctc ctgcctcagc ctcagggcgg atcacctgac atcaggagtt tgagaccagc 90780 ctggccaata tggcgaaacc ccatctctac taaaaatact aaaaaaaatt agccaggcat 90840 ggtggcacgc acttgtagtc ccagctactt gggagactga ggcaggagaa tcgcttgaac 90900 ccaggatgtt gaggttgcag tgagctgaga tcacaccatc acaatccagc ctgagtgaca 90960 gagtgagact ccatctgaaa aaaaagaaaa aacaattagc ctggcatggt ggcaggcacc 91020 tgtaatccct gctacttggg aggctgaggc aggagaattg cttgaacccg ggaggtggag 91080 gttgcagtga gctgagatcg tgccattgca ttccaggctg agcaacaaga gcaagactcc 91140 gtctcaaaaa aaaaaaaaaa aaaaaaaaaa ggccaggtgc agtggctcac gcctgtaatc 91200 ccagcacttt gggaggccaa ggtgggtgga tcacctgagg tcaggagttc cagagcagcc 91260 tggccaacat tgtgaaaccc ccgtctctac taaaaataca aaaattagct gggtgtgatg 91320 gcatgtgcct gtaattccag ctactcagga ggcagagaca ggagaattgc ttgaacccag 91380 gaggcggagg ttgaatgagc cgagattgcg ccatcacact ctagcctcgg cgacagagca 91440 agactccgtc tcaaaaaaaa aaaaaaaaaa attagcttct acctcattaa tcctaagaac 91500 tcatacaacc aggaccctgg agtcgattga ttagagccta gtccaggaga atgaattgac 91560 actaatctct gcttgtgttc tctgtctcca gcaattgggc agatgtgtga ggcacctgtg 91620 gtgacccgag agtgggtgtt ggacagtgta gcactctacc agtgccagga gctggacacc 91680 tacctgatac cccagatccc ccacagccac tactgactgc agccagccac aggtacagag 91740 ccacaggacc ccaagaatga gcttacaaag tggcctttcc aggccctggg agctcctctc 91800 actcttcagt ccttctactg tcctggctac taaatatttt atgtacatca gcctgaaaag 91860 gacttctggc tatgcaaggg tcccttaaag attttctgct tgaagtctcc cttggaaatc 91920 tgccatgagc acaaaattat ggtaattttt cacctgagaa gattttaaaa ccatttaaac 91980 gccaccaatt gagcaagatg ctgattcatt atttatcagc cctattcttt ctattcaggc 92040 tgttgttggc ttagggctgg aagcacagag tggcttggcc tcaagagaat agctggtttc 92100 cctaagttta cttctctaaa accctgtgtt cacaaaggca gagagtcaga cccttcaatg 92160 gaaggagagt gcttgggatc gattatgtga cttaaagtca gaatagtcct tgggcagttc 92220 tcaaatgttg gagtggaaca ttggggagga aattctgagg caggtattag aaatgaaaag 92280 gaaacttgaa acctgggcat ggtggctcac gcctgtaatc ccagcacttt gggaggccaa 92340 ggtgggcaga tcactggagg tcaggagttc gaaaccagcc tggccaacat ggtgaaaccc 92400 catctctact aaaaatacag aaattagccg gtcatggtgg tggacacctg taatcccagc 92460 tactcaggtg gctaaggcag gagaatcact tcagcccggg aggtggaggt tgcagtgagc 92520 caagatcata ccacggcact ccagcctggg tgacagtgag actgtggctc aaaaaaaaaa 92580 aaaaaaaagg aaaatgaaac taggaaaggt ttcttaaagt ctgagatata tttgctagat 92640 ttctaaagaa tgtgttctaa aacagcagaa gattttcaag aaccggtttc caaagacagt 92700 cttctaattc ctcattagta ataagtaaaa tgtttattgt tgtagctctg gtatataatc 92760 cattcctctt aaaatataag acctctggca tgaatatttc atatctataa aatgacagat 92820 cccaccagga aggaagctgt tgctttcttt gaggtgattt ttttcctttg ctccctgttg 92880 ctgaaaccat acagcttcat aaataatttt gcttgctgaa ggaagaaaaa gtgtttttca 92940 taaacccatt atccaggact gtttatagct gttggaagga ctaggtcttc cctagccccc 93000 ccagtgtgca agggcagtga agacttgatt gtacaaaata cgttttgtaa atgttgtgct 93060 gttaacactg caaataaact tggtagcaaa cacttccacc atgaatgact gttcttgaga 93120 cttaggccag ccgactttct cagagccttt tcactgtgct tcagtctccc actctgtaaa 93180 atgggggtaa tgatagtatc tacctcctag gatttattga ggcagcttaa ataccttttg 93240 tatttcctgt tgctgccaaa acaaattgtt gcaaggtcag aagtctgagg tggctcaact 93300 gtttctttgt ttcaggtttc atgaggccaa aataaaggtg ttcgcagggc gtgttccctt 93360 ctagaggctc tgggtccttg cagttctagg actaagatcc ctgtttccca ctggctgttg 93420 gctgggcatc attctcagct tcttgaggct ccccacattc ctaggctcct ggcctgtctg 93480 cctccatctt caaaaccagc aatgggtggt caagtttttc tcacactgaa tcttgctgac 93540 tactgtatct ttctaactcc tgccagagac atttctctgt ttctaagggc tcaagtgatt 93600 agattgcacc cacttggtaa tccaaagtga tcttcatatc ttaaggccca tagccttaat 93660 tatagctgca aagtcccttc gcagcagtac ctagattact gttggaatga ataaccagaa 93720 gacagcaatc aagggaggac atctttagaa ttctgcctac cacttgtatt taacatgctt 93780 aatccacaga tgacactctc taccattatt tcctggtcct cacactgctc agagattgga 93840 atccttttta agcaaagaga atgaagtcat cacatagttc agtcctgctg tatttgctgg 93900 aaacagtgaa ggaagataga gaaaatggag ctaactgcca atattaccat tttataatca 93960 gtcctcaatc atagccctat gaagtgggta tttgttacct cattggaaaa atgggagttg 94020 aatctcaagt tccttgtttg taagatttta ctcagatttg cacagctaaa aatgactaca 94080 tggagaccca aagccacctt tctgttccca tcatcagctt tccatctgcc tctgtcactg 94140 accccgggac agaaggttca agccttaagg gaatttggag agagaactag attttgaggg 94200 gaactcacac tcacttccct tttgggccac agtaggagac agtaaaagca gccccatgtc 94260 aggcaaaggg tcttacagga gtggatcatg gctgctgttt ccacttctct ctggcttccc 94320 agcttatgac tgtgtatctt agttgtcaaa gccttccagt tcatcctcac ctacagcttg 94380 acttcccaag ggcccatgcc agctccctgt ctacctgcca gtgagttgat gagtctcggt 94440 gttagtagta aaggcaggcg ggaagcaagc agaagtgcta ctgggccttg agggtaagcc 94500 aggcctcagc cttctgaccc catcactaat gggttaatag gaaaagcagt atccatctag 94560 tacagcctgc cttttcagga atagtgagta aaagcaaaga tgactaaaat acattaaagt 94620 tttctgtaat tgtctctaag gtctcccaac aaacatatac cccatctgtt tcaagctctg 94680 cataaccttt cccagaagtc aagttcaggc cctggcctca tggtgcctgg cccaggttaa 94740 gagtgctacc tgatgatgga gttaatacac gttgctttga cctctgactt taagatgtcc 94800 tcccactttt ccaccccgca atctctagcc ctctctgggc acagcagcaa ttgggaacta 94860 gttcctgtac tgcctttatc tcattttaca aaacaaactt ctacaaagaa gctggaaagg 94920 aaggaggaga aaggattatc atgcaggcac agggaggggg cctagagaag agctctggca 94980 gattatgtcc ctcttaaaaa atgcaaccag aatcatcaac aaagtatcac ctcaaaaata 95040 tgcaggagaa aaagaaagga atcaatgttg gggtggttgg agcagaagga gccaaactgc 95100 ccagaaggtg tcctctgaag gctgcgagga gcagactagg tcagccccag aggcagatgg 95160 cacacacaga atggcaggat taccggtagc tgcagattta ttgacagaag ccctagagac 95220 tgggcctgct gcccagggaa tgtgggggct cacttatcaa agactactgg aaaatggctg 95280 agccggcaac cccttccact acagtgatgc ctggttttct tgcacagcct gtaactctgc 95340 ctgtaacaag gagaaaatta aagcaacgaa tctggccaaa tagaaaatta aggaaaacta 95400 gaaacagctc ctatggagag cagggattgg ggaggtgtag aggggctgat cctgaatgtc 95460 tggaggatca ggaaaatgta agcaattgtt taagggactg gtaggaatca agatctggag 95520 agagatcctc ccgactctgg tggctgggga atatgaactg tggagacatg gtttcaagga 95580 ctcaaaatga tatgacagct taacatttac agttcagtgc agaggctctc aaagcatgat 95640 cccctgatag gagtgtgagg gggcaacacc atcacctagg aatttgttag atatgcaaat 95700 tcccagaccc actgaatccc agacaggtgg ggccagcaac ctgtgaatct acaacaggct 95760 caagtttgag aacaaatgac ttagtgtaag gggctgctaa ttgatataaa atgttacctg 95820 tggtctatta ttttgtctgt agtgaatatt gggcttgtta aggataaata aggtttgtgg 95880 gctggtaagt ggttcttctc tacaaggttg caacagctgg cttcagttaa cttcaaaaag 95940 gccctttaag caaagacagt agtcccccca ctcatccatg gttttgattt cagttactta 96000 tggtcaacca tggtccaaaa atattaaaag gaaaattccg gaaaccagtc actcgtttta 96060 aattgtacac cattctaagt attgtttgac ttgttctatt ttattattag ttattgttgt 96120 taatctctta ctgtgcccaa tttataaatt aaattttatc ataggtatgt atgtataggg 96180 aaaaacataa tatatatagg gtttggtact atccgagggt tcaggcatct acttgtggtc 96240 ttggaacata tgccccgcag ataagggggg actgctgtac aatgcaaagg acaaagatta 96300 aattatatta gcaatctagg agcagaaggg caagactgct tttttaaaaa acagctaaag 96360 gtttaggagg ttttattaat atttaaattg tattgaaacc acagctgcag cctttgactc 96420 cagcatagag atatgcaaat atggctttca aaagaaaggc aatttcagac agccctcaaa 96480 gtaacaggaa caaataaaac aaatgatttt gtaatttatc tttattgact gatgttgcac 96540 aaggcacagg ccataccctg tgagagtcag caacagccga gctctctgag gagagaagag 96600 aaagccaggc tggagggaga ggcaggccga cccatagaca ggtgacagga aagacacaga 96660 gcaggcagat gggagaagaa gacaactaaa ttaaaaggga aggaaaataa aaacccagcc 96720 ctgggtcctg tagaccatct gatcttgctg gctctcagca gcaacaacaa taatcattaa 96780 tgactatcat ttgccacact actactaagt gccatgcact attcctcaca tacaaatgag 96840 gaaaatgaag ctttgagagg tcaagcaact tacccaaggt cacacaacaa aaggaagggg 96900 cagagcccag attcaaagat ttgtgtgagg ctgaagccct gtgctctttc cagtgcatta 96960 tgctgggaac cagtcctggg aggcagtgaa taacaataag gttaatgggc cgggcgcagt 97020 ggctcatgcc tgtaatccca gcactttggg aggcggaggc gggcaaatca cgaggtcagg 97080 agatcgagac catcctggct aacatggtga aaccctgtct ctactaaaaa tacaaaaaat 97140 tagccgggcg tggtgtcggg cacctgtagt cccagctact caggaggctg aggcaggaga 97200 atggcatgaa cctgggaggc agagcttgcg gtgagccacg atcgcgccac tgcactccaa 97260 cctgggtgac acagtgagac tccgtctcaa aagaaaaaac aaaacaaaac aataaggtta 97320 atgattgagg ggacactttg tgcccagttc tgtggtattc tgtatgggca tgcgtgtgtc 97380 tgtgtgtgtg tatatgtatg taactgtgga aaagagggtg aaaacctcca tttctgacct 97440 tcaaattggt tactatccaa tgagtaaggc aagaaaagaa agccaaagaa aacttgcaga 97500 attctggtgt aaaagttctt ttggggccgt gtggtggggc cagctctgcc tgttgtggaa 97560 gacttctggt ggaggcatct cagctggcct tggccttgag taaaatttag ccagatgaaa 97620 aggaaagctg gagattacac aggcccaggt gagagcctcc agctgctaga attggaggaa 97680 ggagcacctg attcagagag atgagaaaag gcaagagaat cctgaaagga tacatatctc 97740 tgaccctttg tccccatcca atctccccag accttccatc ccaagcccaa acacaacctt 97800 acctgctgct ccttttcagg caccctggcc accaaatata ggaacccata aattttgctc 97860 atactctatg ttctactagg caagtcctga tctgtcatct ctacaggccc caatccttcc 97920 cgctcacccc tacagagcct tctccaggtt ttctaggcca gaatctctcc ccacttagaa 97980 tactccagaa gttttgcttt atttgtgaga ctttattcaa ttgaagttac ttgtgtgcat 98040 atgttatcct ctctatttga ctagaaggtc cttataatcc cttatgacca taattatttt 98100 atctttgata taacccagct ctgtaactag cagatacttt gttaggcatc cagtgggttt 98160 ttcctaaatg aatgaagtaa aggatgaatg aatggactca gtgcattgaa gggcttatcc 98220 aactattggt tccactctca agacctttgg aaaactagcc atgttctgga atgctaattc 98280 ccttcaatgc ctttcgccca tttttctatg accctgattt actccaaaaa caatataagg 98340 gatctaagtg tccaagaatg actccttcta aacccacacc taaggatttt ctctcttttt 98400 gtgtgtgtgt gtgtgagaca gagtttcact cttattgccc aggctggagt gcaatggtgc 98460 gatctcagct cactgcaacc tccgcctcca gggttcaagt gattctccct gtctcaccct 98520 cccgagtagc tgagattaca ggcgcctgcc atcacaccca gctaattttt gtatttttag 98580 tagagacagg gttcaccacg ttggccaggc tggtctcgaa ctcctgtcct caggtgatcc 98640 acccaccttg gcctcccaaa gtgctgggat tacaagcatg agccaccaca cccggcctct 98700 ttgattctct tttgcctatc atgaagtcta cccctttgta attaattaga ccaatgtcca 98760 cccagacaga ataacatttt cccctatcca tcagcgaggt cttctccgtg atggacattc 98820 aaggcagaca gagagactgc tgctgcaata actggggaaa taattatggt gttcatgatg 98880 atttctttgc aggttcaaag cactagccca gccattatct ctcccacttc actaggataa 98940 aattgctaac cccactttat aggtgctaaa acaggtccag ggccttgtca aaggtcactc 99000 agtgagctgg tggcagacct ggaaataact agcctaggag tctcgatatt cattaggcca 99060 cagatggaaa tgccctcatt atgctgtctg ggctatgtct gagagagagt caactaactg 99120 gactccagtt aaatggagat atgcactgga agataagttt gtgactacag agtgtttttc 99180 tctgcaatgc tgcagcagtt ggcactggtt aattccagag ggtgtgtgtg tgtgtttgtg 99240 tgtgtgtgtg tgtgtgtgtg tgtgtgttta aagcattatc acgcgtccta gatgagggaa 99300 gagagggtga atccaaggta acacagacac acaggtaagc agatgtttgc catcttctct 99360 tgaaagtcat ataaaaccaa atgacagtgt atattagcag gagaaactca ggaggctctt 99420 cccagctgtt aggctatacg actctggaat aagctagtac aaattaggta gaaagtctag 99480 gattgttcct agagcctggt ggcgggaggt ctttcctgga ggcaaaggac tgtggggctg 99540 tctcagggcc ttctgcagct gctaaagtga gaagcctgcc gacgggatca tccccaagcc 99600 cacagaagct ctgaaagcta tggaaaccaa gatctgtaca ggagccactt ctggtttcta 99660 atgcctgaga gattaaaatg gaaaaaaaaa ttcccatgga aattcaagaa tgcaagaatg 99720 ttctggggcc aggcacggtg gctcatgcct gtaatcccag cacttttgga aggccgatca 99780 cctaagatca gaagttcaag accagcctgg tcaacatggt gaaaccccgt ctctattaaa 99840 aatagaaaat tagctgggcg tggtggtgtg cacctgtaat cccagctact caggaggctg 99900 aggccagaga atcacttgaa ccctggagcc agaggttgca gcgagctgag atcatgccat 99960 tgcactccag cccaggcaac aagagcaaaa ctccatctca aaaaaaaaaa aaaaagttct 100020 acaacgtggc cacaggtccg ttctggctaa ggcagtgatg tccccctccc accaaagccc 100080 aaaccttcta acatcatcct aaagtgtggg aatcacctct tcacctcagg ccagctctgg 100140 gcttttctca gcctattcat cagcctccat tagtcctcag ctctgctgag gcctcagcag 100200 cttcccagtc ccactgaagg ctgtggggca tagaatgggc agagggcagg ccgggcgtgg 100260 tggctcaagc ctgtaatccc agcactttgg gaggccgagg cgggcagatc acgaggtcag 100320 gagatcgaga ccatcctggc taacacggtg aaccccatct ctactaaaaa tacaaaaaat 100380 tagccaggcg tggtggcagg tgcctgtagt cccagctact tggtaggctg aggcaggaga 100440 atggcatgaa cccgggaggc ggagcttgca gtgagccaag atcctgccac tgcactccag 100500 cctgggcgac agagcaaaac tccgtctcaa aaaaaaaaaa aaaaagaaag aatgggcaga 100560 gggcataaaa cctgagtcca gaggtggtgg ttgcacaaca ttgtgaatgc actaaatgcc 100620 cctgaattgt acattttaaa atggctaatt gtatgttatg tgaatttcaa tcgattttta 100680 aaaaaaataa aactgagcca cctttggggt ggggagagga gctgggccag gctctgagga 100740 tttgagggtt gaaactcctt gcagggagtg aaatgaacga caatggggag gccagtctgg 100800 ccctcccaac tcctcctcca ggaccagatg ggaactgggg ctagggagaa aggcccaact 100860 ggggcggcgc cgggctctgg gcagaagaga agcactcagt gaatgtgagg aggctgcagc 100920 cgtcggctca tttgcatcat aagtgattgg ttttccctgc tcgtccctca tcaggacaca 100980 atggacagtt gtttgctggc gcagcagatc catttaccaa gggagagagg agacagagca 101040 caagtgaccg atgggtaata gtgttgaagg gtgggcagcc gcctcccctc ccctgtgctc 101100 ccaggccact gggactcttg ttctcacaca atgagaaggg accttagaga gcaaatcacc 101160 gcttcacttt atagaagaag agactgaggt gctgagagga ggtgagcctt gctgtggtca 101220 aacagcaaga acatagcaaa actaagcatt ttaaactcta acctctggat cctttttctt 101280 tgagacaagg tctcgctctg tcacccaggc tggagtagta cagtggcaca atctcagctc 101340 actgcaacct ctacctccca ggctcaagtg atccccccac ctcaactttc tgtgggccac 101400 gacacctggc taattttttg tagagacaag gtctcactgt gttgcccaca tttttctcga 101460 actcctgggc tcaagtgatc ctccagcctt ggcctcccaa agtgctagga ttacaggtgt 101520 gagccacagc actgggcctg tttggttttt gttttgtttt gtttttttga gatagggttc 101580 cactctgtca tccaggctag agtgcagtgg tatgatcact gctcactaca gcctcacact 101640 cctggttcaa gtgatcctcc cacctcagcc tcctgagtag ctaggactat aagtatgtgc 101700 caccacgctt agctaatttt tatttctttt attttttcta gaaacagtgt ttccctatgt 101760 tgcccaggct ggtctcacct gggttcaagt gatcctccca cctcagcctc ctgaatagct 101820 gggattacaa gtgtgagcca ctgcaccagg cctggattct aaactgtcat ttgagggttc 101880 acttcgtttc cccataatac cttctctgtg cccttattcc catctctgtg gtctcctgtt 101940 cccggggcct tcgtttccat cattctgtct cctgggtcta tttctttttc tctgtttctg 102000 ttcctctctg tatcttttcc tcttggtttc caggcagcta ggataattac tagactttta 102060 attaacccct gccctaacaa aggtgggtct ggcatgaggc agcaatttag caagtgtctt 102120 ggtttgtttt ggggataggt ggggagagaa aaatatgtgt tggggcctat tataaaccag 102180 gcactaagac agacacataa tgcactttat ctcatttcat cctttcaatc ttgcaaggta 102240 ggtgttctta gagacaaaaa gggtgaggct cagagaggtt aagtaacttg tgcaagggca 102300 cccagctagc aaattgtagt tacctgactc caaaacctct gttcttccat ctcacaccct 102360 ggcacagggt ctaactcagg gtaaggggct cattgatttc aggcgcaagg gaggcacaaa 102420 gtcactgaag gagaccactg ttttgttgct gtcctctagg cagcgactgc gtccccccag 102480 agccccctcc ttctctgagc cccttctgca gcgtggcgaa atctcacaaa tgcaagcttt 102540 tgcccccagg gaggtgggga ggcagtgatc aagaaagaaa cctgacaaac ccagaccaac 102600 catgggggtc tccctcctgt taacacccct ccctaacagc cctcctggtg gttccctgtc 102660 tgcccctccc ctttatgggt caagcctgct ggcgtctgtt tcattgtgct gtgggggaag 102720 gggagagtca ggggtgagtg ggtgtctgtg tgcatgaaca taaggcctcc gggttcattc 102780 tgacactgaa tgaaaaactc accaattatt cgtccagtct cattaatatg cagacagaca 102840 tctgttattt aggagtcaac agcagaggca ttttcttgtc gggaggggca ctagtgtaca 102900 gggctctctt gtctctccgc tgctagcggg tagctactca ggaatcatcc cacacctccc 102960 gacctggagc ctcccctctc tctgaccctc actcacagct ttgaggacag caagtaaggg 103020 attgaccaga cagagatgga gggagatctg ggaacctggc tggaaggaag gaagcaggag 103080 aggagctgcc ttgtgtagaa caaactgaga acaaaacgct aaaccctttc ctggggaaga 103140 gaatgtggag ttgggggaga gagctgtgcc aagagtgcct gccccactgg gaatctcagg 103200 gacatgaccc ctccccccac accttcctca gcctgcagga caagtctgag tgcatctgaa 103260 gcagggagag ggtcactatg gcaacatgaa gtcctcaccc agagactgca gaaaacgtaa 103320 taagaggagt tcagaaaaat ggagaccaag ggacctcaat cttttttttt ttttttcaat 103380 ttatttattt ttttttattg atcattcttg ggtgtttctc gcagaggggg atttggcagg 103440 gagggacctc aatctttgga ggagtcacta aagctctctt caggccccaa gataggggtg 103500 ggaacaagac ataaccacct cctgctttct gtcttctgtc ttcctccagc ctttaagtcc 103560 cagcacaaaa tacccctcca agaagccttt cccaactccc tcaggcccag cttagaagca 103620 cttaagcctt ggtgtcttgg ttgtaaagaa taaaagttga catcagctga gcaacacaat 103680 gaggtagatg tggtgatcag cccccttttc taggtgcaaa aactgaggtt cagagaggtg 103740 ctgggcctca ccaaagattc cccagggaag aagcagcaga gctcaaccca ggccctggga 103800 cttctgcctc tgaacctgaa gctcttccca cgactacccc ctgggagggc cagagtcaca 103860 aggggaggac ccttgtcagc tgaagtgttt caggagtttg attgagtcct ctcttcccat 103920 ccaccctgtc cttccccctc ctccctccta ggcaggcgga ttgcctaggt taagaaacac 103980 tagtctgggc gaggtggctc acgcctgtaa tcccagcact ttgggaggcc aaggcaggtg 104040 gatcactagg tcaggaaatt gagaccatcc tggctaacac ggtgaaacct cgtctctact 104100 aaaaaataca aaaaattagg ccgggcgcgg tggcttatgc ctgtaatccc agcactttgg 104160 gaggccaaga caggcggatc acgaggtcag gagatcaaga ccatcctgac taacacggtg 104220 aaaccccgtc tctactaaaa atacaaaaaa tgagccggac gtggtggcag gtgcctgtag 104280 tcccagctac tcgggaggct gaggcaggag aatggcgtga acccaggagg cagagcttgc 104340 agtgagccga gattgcgcca ctgcactcca gcctgggcga cagagcgaga ctccgtctca 104400 aaaaaaaaaa aaaaaaaatt agccaggcgt ggtggcgggt gcctgtggtc ccagttactg 104460 gggcggctga ggcaggagaa tggcgtgaac ctgtgaggtg gagcttgcag tgagccaaga 104520 ttgggccact gcactccagc ctgggcaaga aagcgagact ctcaaaaaaa aaaccactag 104580 tctgggcgcg gtggctcctg cctgtaatcc caacactttg ggaggccaag gtgggtggat 104640 cacctgaggt caggagttcg agaccagcct ggccaacatg gtgaaacccc atctctacta 104700 aaaatacaaa aattaggtca ggcatggtgg ctcacgcctg taatcccagc actttgggag 104760 actgaagcag gcggatcatg aggtcaagag atggagacca tcctggccaa catggtgaaa 104820 ccctgtctct actaaaaata caaaaatggc tgggcacggt ggctcatgcc tgtaatccca 104880 gcactttggg aggccgaggt gggtggatca cgttaggtcg ggagttcaag actagcctga 104940 ccaacatgga gaaaccccat ctctactaaa aatacaaaat tagctgggca tggtggcaca 105000 tggctgtaat cccagctact tcaggaagct gaggcaggag aatcacttga acccaggagg 105060 tgaggttgcc gtgagccgag atcgcgccag tgcactccag cctgggcaat aagagtgaaa 105120 ctccgtctca aaaaaaaaaa aaacactaaa attagctgtg catggtggcg cgcgcctgta 105180 gtcccagcta ctcaggagac tgaggcagga gaatcgcttg aacccaggag gcagaggttg 105240 cagtgagccg agatggtgcc actgcactcc agcctgaatg acagagtgaa actccgtctc 105300 aaaaaaaaaa aaaaaaaaaa aaaaaaaaca cagaaactct ggcagccatc acagtgtgat 105360 tatttgttta tttcattaaa tgtttaacga ggctacattg tttcccaaac caatgtctaa 105420 tttgtgaagg aaacagcgca gagaaggaag ctgggtgact cctgcatctg gggtggggaa 105480 gggagtaagg tcccctccct ccatcctaca gaggcctttg aggatcagca acagtcccat 105540 tccctcctcc cacccactga gctcctcagc ccagagccct cctccccaga aataaaacgt 105600 ctggcaaccc agacctgcag aaagggacca aaaatccatt cctggtggta ttgaaaatgt 105660 attaaacttt ggggggtcct ccagctgatt gatttttcta attatgtttg ctttagatgg 105720 atatttaaat gcatttgcat tccctgagct cacatggcag gatatggagg ttggaggaaa 105780 gagggggcac aaacactcca cactctgcac tttggtggtt gcaggcttga acctgctata 105840 cactgagaag tccaaagtgg aaaagagaag ccactcagct aaaaatcgca agtcgatttt 105900 tatggcaggt ccttgtgggg aaagggtcag tcctcagaga cagatggaga tccacctagc 105960 tgggcctgga gcccctgccc tctcctgtac ccttagccga ggactcaggg tctttgagtc 106020 agtccctaac caggtctcag tttgaggggg tggttatcca agcacactta gataatttca 106080 aatgccattg aagttatcct agaatctttg agactggctg agatgaacta gtcccatagg 106140 agaggttggg atagggatat ctgatgatcc agggagtggt gggtagggat tcctttcctc 106200 tcaagactgg aacctggcat aagggaaagg agaagctatt ttttattttt tattttttaa 106260 ttttttttag agacagggtc tcactctgac actcaggctg gaagacaatg gcatgatcat 106320 agctcactgc agtctctaac tcctggcctc aagcgatcct cccagcttgg cctcccaaag 106380 gaggaatctt ggctgggatt ataggtgtga gccactgccg agaagctatt attttaaatg 106440 acacacctca gagccaaatc tcccagctcc aacaccacat ccagataacc atctatccaa 106500 aaaacaactc tgatcacttc actctctgcc tgaaattcct ggtggcttca tcctctgagg 106560 atgatttcat tcatcctcag aatgaaattc tgattcctct gtggaccctg cagtagcctc 106620 agtgtacctt cctagccttg tcttctattc tccctgccat gggagcccca acagtgctat 106680 gctcattctc atctccacgt gtttacacat gctgtaccct ctgcccagag tgcctttcct 106740 accccttccc tgcccggaaa actcctcttc aaccctcagg acctggctca caggactggc 106800 ttctcaggct gcaaggagct cccatagcat cccatacatg tacaaatatc cctcagccat 106860 ggcaccctca cacctgaggt acctctcttc cacactgggc tggcctccaa aagcttagag 106920 actggtcctt gcaatctccc aagccagtgt atgccacaca gttggtgttc agtacatact 106980 tgctgaatga atgaatgagg gaggaatggg ctataaattt gggtgggatc ccagcagata 107040 gttgggtaag gtcagtgttc tcttccagtg tgtctgggag aactggctag ggctggggga 107100 gggaagggcc agggatggtt cctgggggag aatgtcaccg aaaagaggcc agtgggacca 107160 gagccaggaa gggaatacag gacaatctga aaccagactc ccgagaaaac agaccagtac 107220 tgtctttcct gacaacaggc gctcagccgt cctctccacc gtctttcctt taagggacag 107280 ggtaggggtg actctaacag ctgatgctcc cctgaaagcc atcatgaaac tcagcatggg 107340 aggagagaaa ggtccctggc ctgagcctct aaggagaccc cagaatcaaa ctactgacct 107400 cttaggaaac ttcacgctgt acaggggtag cttctgtgat gtggaggctt ttgatgcctt 107460 cttttttttt tttttttttt tttttggaga cagagtcttg ctctgtcatc caggctagaa 107520 tgcagtggcg caatctcggc tcactgcaag ctccgcctcc caggttcacc cgggttcaca 107580 ccattctcct gcctcagcct cccgagcagc tgggactaca ggcactgcca ccgcgcctgg 107640 ctaatttttt gtatttttag tagagatggg gtttcaccgt gttagccagg atggtctcga 107700 tctcctgaac ttgtgatccg cccacctcgg cctcccaaag tgctgggatt acaggcgtga 107760 gccagcgcgc ccggcctgat gcctccttat ccccacaacc cccagggtac cagcaggctc 107820 caagccaggg gtacagatgg tgagcaggac ccctcccaca ctagcagcag gcctggctgg 107880 gctgagaaat gctgactaat tatatgtcgg tctgctctaa aaccccctaa tggcctgaga 107940 attgcccact tcattaacta ggatgaacag tcccaggatg tctccttctc ccaactctga 108000 ctcctaaaag gacacttctg atccaaccta tggctttgtc ctctgctcta tctgtggaca 108060 tggacaggaa agttccccag ctgaggtcta actttccctc ttactgctaa agattggtag 108120 attgattttt ttaaaaagca acaaaactaa agccacagcc gttttccatg gaggtgggct 108180 ttattaggtg actgttgagg caagggaggt tctagggctg gtggactgat ggggggcaag 108240 ggcttctcct tgcttttgaa tttagtgcat gttgcctaga ggttagatgt gtgagaatag 108300 ctgcagaagt gagaggagag gaaaagagaa ggtcatagaa tggacatttt ccttgggcca 108360 gaaccaggat atggggactg ggggtggaga gggagggtac tcttcacata ggagactcca 108420 ccaaggtcac catttgatac cagcttccct aacgcccacc tgccccatcc cagttcatgc 108480 cccagatgcc agccctgtta gctccctcaa catccactgg agaagaggag ggaggaggag 108540 atgagaaacg atgataccct tctgccctcc agctcccctg cccagaattg ctcgctctgc 108600 ctgccctaac ttcccagcca ggatcaggag gtcaggaagc ctgggcgcag gcaggggaac 108660 aattgtgtcc ctcaccaccc ctcttcacac tctgccctct cctagcccct cacatgaggt 108720 tgcagctttt ggctcgatcc ttgtgtatct cgccctcatt cccccggtct ggccgtcctg 108780 acagctgagc ggatcgctgc attccccggc gtgagtcagt tcggcgcagc tgcctatggc 108840 cacggccaag ggaggccact gtagccacat ggaagacatc cctgacgctg cgctcagagg 108900 accgggagga gcactcaaca taggacacag cccccacctg cttggccagc acagtgccct 108960 ggaaaaggaa ggagtgcatg ggagaaagtt ataggtctta gcctgcagct tagaaagggg 109020 catggaggct gtgggctggg gttgaatgtc aaggctgggg gcagtcaagg gatcaggtca 109080 gaggtcacag accagaacaa aggatgagcc aggtaaggtg ttttcaaatc agagactgaa 109140 ggggcagagg tgacaggtct aggctgggat gaggtcagac gtcaagggtc ccacctgctc 109200 atgtgtaaca gggataagcc tctgcttgga cagctccctc agtgtggcca ggtcagtccg 109260 catgtccagt ttacagccaa ccagcacaac cttggcattg gggcagaact cttgagtctc 109320 tccttgccac tatgtaggag aagaaaagag aattgtggag gggtggaggg aggcacagcg 109380 tgagcctttg tgccatgcca gcagtgtgcc ctctcttcct caagcacgca gaaaccatgt 109440 atccctcagg actctcccac atgaggaagg aggtgagaat gctaggcttg gtttgagagc 109500 aggatggggt gagagagaag cagcggggag gagagggctg gcgtgggcct gtggactctt 109560 ctccctcagt ggctatgaag ggtctgccag cctggaaact tcccattccc actcgccttt 109620 cccatactct ctcctgggaa caaatttatc ccaccctccc ctcccccacc tgggaactgg 109680 ggctgcccta gctgacttct gtccattcac ccctggcttt tgtcatggaa actggggcct 109740 ggagaggagg ccacagggct ttcctgagct ccaggatcag gcttcccatc ccatcccctc 109800 catctgggac tcccactgcc aaggagttgg aagagcagag aaggaatcct gtgagtgctt 109860 ctcccttcac tcccccacct cccctagctg ctgtatccag ctctgaggac tttcaggaaa 109920 ggggtggctg ggagggatgg gggctggagg caggggtggc agggatgaga gcttcactcg 109980 ctaaccagct gatggccata ccccagccat cactccctcc tcctggccca tgttatgtca 110040 ggaccatggt ggtctggtcc ccctcagtct agctgcccta tttccccagg ctcccacctt 110100 cttgagaaca ctgtccagtg tttctggtcg gctaatgtcg aagcagatga gcacagcatc 110160 agaatcagga taggccagag gccggacatt atcatagtaa gaggaacctg aaggaagaca 110220 gggcatgagg ggcctgagtg gatgggaggc ctggaaggga atgggagacc ttacagatcc 110280 tggtcaaggg atgctgggag cagagaatgg aaaagagcaa ccattaatac ccatcattaa 110340 tacccatcat ggagtctggg tttcccaagt gggggagcgg gcagaaggga ggtcacatgg 110400 tgggaaacgg ctctctgctt ccctagtggt ttaaaaagta ataattttta ttcttgactg 110460 aggtttggac ccctttgaga agctcataaa atctatagac attctcataa aatgttgcat 110520 gtgctttctg ggctttggca gtctaaagcc ctgaagggaa ctcttgtaaa aataaaaacc 110580 ctccttatgt tgggaggagg aaaagagcag tggcagggag agcactctcc cattctcctg 110640 ggacttgacc tcagatttat ctagttcaat ggagagaaac agcctcctga ccacccctca 110700 ctcaagacat tctaaatgtc ttttctgctt ttttattttt tgagatggag tctcgctcta 110760 tcgctcaggc tggagtgcag cggcatgatc tcggctcact gcagcctccg cctcccaggt 110820 tccagcgatt ctcttgcctc agcctcctgg tagctgagat tacaggcacg tgccacacgc 110880 ccgattaatt tttgtatttt tagtagagac ggagtttcaa ccatgttggc caggctggtc 110940 tcaaactcct gacctcaggt gatcccccca ccccagcctc ccaaagtgct aggattacag 111000 gcgtgagcca ccgtgcctgg cctctaaatg tcttttctaa acccagtctt atctctgaag 111060 gaacatgttc caaattaaaa gccattcctt cccaactttc ccaggtaggc aggacccagc 111120 tgaggggctc agatcctagg ctttctcctt caggacatgg tttctgtcag gctctgcaag 111180 ttctacctca gtttccctgg attttagcag aatattgatt tttcccttcc tgttggaatt 111240 ggatggatgg gctgggctta cctggaacct aagggtctaa ccaagggagg ggacagagtg 111300 ggccgccttg gaagtcaggg tgacccccag ggacttggct acctgaagtg tcccacatgt 111360 tgagctcaat gcggcgcttg tcgatctcaa agctcgcagt gtagttctca aacacggtgg 111420 ggacataact ctgcagacac ggatggatcc agatgagatc atctctccaa gtcctcaccc 111480 cagataaatg ccctcctcac tcccacaccc cgtccagccc agcccctgga cacaagttgg 111540 tctgggattg ggcaaagggg agatcccggg agctcctgcc cccccccccc cccccccgga 111600 gaatctctgc taagctccaa gacctcctcc tgttcccttc tggtcccttc agccccctag 111660 ttcttcccct ctccattgcc caggacctcc gacattcccc tcgccctccc tcccggatgc 111720 tctggttctc ccaaacccca tctatctcac cctgctccct aattcctccc accccaatcc 111780 tctgcagtcc ttcctgagcc ctcaaggcct ccccgcgtcc tccgaccccc tgtctcttgt 111840 ccctggttac ccgagtaccc attcccatcc gtcgccaggg cccctgtcac ccacccccca 111900 gcagccttag cgtccccctc ccaagacgca ggtccctcac cccgggatag gcgtccttgg 111960 cgaacacctg cagcagcgcc gtcttgccgc actctgcgtc tcccaccacc acgatcttgc 112020 agcggccgct ctgcccctcc atggtcccgg ctacgagccg gtcccccacg ccacccctct 112080 cccggtcccc tccttcgcct ctcccgcccc tgcaactgca gccgctcggg ccgccaacac 112140 cggcatctcc cgggcccgcg ccgagccccc gccccgggtc cgcggccccc cctccgcccc 112200 gcccccagcc agcgccgcgc cccccggccc tcctcccacc cccgcagccg gggtcggggc 112260 cagaagatct ggcggagccc tgggaacaga ggcctcagag ccggggtcca gcccgccggt 112320 gtggtctgag gggcccctgc cggtttggga caggccgaac tgggcttatt tgactttctc 112380 ggatataagg gcaggtcaga gttcaagcga agttcttagg ggtagaatat gagcggcaca 112440 agcgcgaagc tcgggcctgc tgtgtaccca cgcgtgcacg caggtgtacc agtgcggaca 112500 agagctgggg cagccatcca cttcctgaac acggcgggag agagatgcta aggggaagga 112560 gggagcctct ttggttttct ctcccgcgtc cgcctatgtc ctggcagggg gtcttgggga 112620 aatgggaggg tgaaccccag cacacccacc cggacggtgg tgacatcata gctttccgtc 112680 cccatggcaa cgggcagccg ggtctccggt tacattgact taaccgccgg cctagactag 112740 cagagaagcg tggactgagt tcctccagcc aagcactggg tggaaagttt tgggggagct 112800 gcgtcctctg gtggatgctt ggggacaagg agataaggaa gagaaagaac caaccgccag 112860 agttgctctg ctggagccag agctaaaccc aaaagtcagg cttgattaag agtctgacaa 112920 taggccgggc gcggtggctc acgcctgtaa taccagcact ttgggaggcc gaggcgggcg 112980 gatcaagagg tcaggagatc gagactatca tcctggctaa cacggtgaaa cccgcacggt 113040 gggcgcctgt aatcccagct actcaggagg ctgaggcagg agaatggcgt gaacccggga 113100 ggcggagctt gcagtgagcc gagattgcct cactgcactc cagcttgtgc aatagagttt 113160 cgaaaaaaaa aaagtgcttt tttatatcga ggcaattcga gtcaataata tatgctgcaa 113220 ataattctgt aaagataact agaagctggg cgcggtggct cacgcctgta aactcagcac 113280 tttgggaggc caaggcttgc ttgcgtgcag gagtttgagg ccatcctggg caacattagc 113340 gagaccctct ctctagaaaa aaaaatcaaa acttagctag gtttggccac tctaggcacg 113400 ctgcctatgg ggtagccctg ctctgcaaag agcagtaaaa cataaagtta gccgggcgtg 113460 gtgacacatg cctgtggtcc cagctattca ggaggctgag gtgggaggat tgcttgaagc 113520 cgggagtttg aggctgtagg gagctgtgat cgccccacct cgctcagcct gggtgacaga 113580 gtgagaccct gtatcaaaaa aataaaaata taaatataac tagagcacgc agcatcatca 113640 ctatgttaca gaagggaaaa tgaggaacag aacgttaaca ccaaagtcag aaagttttaa 113700 aggcttggtc tccatgcttc tactttgcca ctgcaagacc acagtgaatt aagtctcatc 113760 cctgcctggg ttagatgtca gagcctgaga cacaatgtag ttggactcca gtccacaggt 113820 ggctgactcc aaatctgata tgagttaact ccaaatctga tgtaagttca agttttggga 113880 ctgttcctta actttttttt tttttttttg agacggagtc tcgctctgta gcccaggctg 113940 gagtgcagtg gcgcgatctc gactcactgc aagctctgcc tcctgggttc atgccattct 114000 cctgcctcag cctcccaggt agctgggact acaggcgcct gccaccacgc ctggctaatt 114060 ttttgtattt tttagtagag acggggtttc accgtgttag ccaggtgaat ctcctgacct 114120 cgtaatctgc ccgcctcggc ctcccaaagt gctgggatta caggcgtgag acaccgcgcc 114180 cggccttttt ttttttcgag atggagtctc cctctgtagc ccaggctgga gtgcagcggc 114240 atgatcttgg ctaactgcaa cctccgcctc ctgggttcaa gcaattctcc agcctccgcc 114300 tccctagtag ctgggactat aggcacctgc caccatgcct ggctaatttt tgtagtttta 114360 gtagagctgg ggtttcacca tactggtcag gctggtctcg aattcctgac ctcaggtgat 114420 ccacccaccc gcctcggcct cccaaagtgt tgggattaca ggcgtgagca cggcgcccgg 114480 cccttttttt tttttttttt aacagggtct cactctgttg cccagactgg agtgtagtgg 114540 cgcgatctcg gctcacctcc gcctcccagg ctcaagcgat tcctctgcct cagcctccca 114600 agtagctgag attacaggcg cgcgccacta ccgcccggct aactttttta tttttagtaa 114660 agacggggtt tcaccatgtt ggccaggctg gtcttgaact cctgacctca aatgatccac 114720 cagcctcggc ctcccaaagt gctgggatta caggcgtgag ccaccgcgcc aggcctatcc 114780 cttaaaatag tttttaattt gaataaggtt tactatgaat aaataaatca cagtcggctt 114840 gatcccaaga gcacagacgt tcctggtgcc ccttttcgtg ctctcccagc ttgcgccact 114900 atggccctgg ccctttaagg ctgagcgcga ggccccgcct cgcccggcgc cccgcccctc 114960 ccgctggatc ccgcagccgc ggctcttccc gacgcgttcc gacttcccca gctgtgcact 115020 ctccatccag ctgtgcgctc tcgtcgggag tcccagccat gtccgacgag agagaggtag 115080 ccgaggcagc gaccggggaa gacgcctctt cgccgcctcc gaaaaccgag gcagcgagcg 115140 acccccagca tcccgcggcc tccgaagggg ccgccgccgc cgccgcctcg ccgccactgc 115200 tgcgctgcct agtgctcacc ggctttggag gctacgacaa ggtgaagctg cagagccggc 115260 cggcagcggc cccggcccct gggcccggcc agctgacgct gcgtctgcgg gcctgcgggc 115320 tcaacttcgc agacctcatg gctaggcagg ggctgtacga ccgtctcccg cctctgcctg 115380 tcactccggg catggagggc gcgggtgttg tgatcgcagt gggcgaggga gtcagcgacc 115440 gcaaggtgag cgggttgcgt agggcagggc agggctgcgc aggccactgg gcagtggggc 115500 acgagtgggc gagcgccggg ggtgtggcag ggcgggagaa actggcgcgg acctgggtgc 115560 acgagcgtgg aaagcgtagc caaggaactt gtgtttgggg gctcctggag agcggcattt 115620 atgtggggag gggagacgaa attatcgccc cttccccaac cattttaagt tgtggccgcc 115680 gcccagaagc tgtgctggtg ggggggaaaa caataaggtg cccatgcgca tgcgcacaac 115740 cacactaccg tccccaccca cccccccccc ccccattaaa accacacctg tacccctacc 115800 caccaaacac tctctgggta attgtggtct gtgactatga gtgacggtta gtgccccctt 115860 tccccgaggg agcttgaggg gctatgtcgt cggggttggg cgggggcaca gcggccgtgc 115920 cagagtcctg gtcacatgca gccccgtggt ctgtgggggt gtgaggcggc ccctcccaaa 115980 gcaaggccaa agagacgaga cacgcccatc acggaggaga gagagccttt gctaccccac 116040 cgccaccagc cttacaccgc cgatctgatt ttggggtggg ggaggcggga ttgggtcatc 116100 cgatctttgt cttgggctct gtgtctcccg tgactgcagt atctcctcct cctgtgactc 116160 agccctcagc cttcgggcca cgacccgggg ctgcccttgg gaatgcctgg ggcggggagt 116220 ggaagggggg acccacctct gccttcctcc tgcagaggac ccccacttca gaaaccccag 116280 tgccaggggt ttggactgga acggagaggt gcggcgcctt gaactggttg gccaagtctg 116340 caggcctgtt tctccttctc atttatcatt aatcttggcc acaaccctgg acaccagaga 116400 gctcaaaatg atcagctttt tgagagacct gggatgaggc ctcagcacgc catttgttta 116460 gaggtttctt ttttttttct ttttcttttt tttttttttt ttttttagac ggagtttcgc 116520 tcttgttgcc caggctggag tgcaatggcg cgatctcggc tcaccgcaac ctctgcctcc 116580 cgggttcaag cgattctcct gcctcagcct ctcgagtagc tgggattaca ggcatgcgcc 116640 accatgcctg gctaattttc gtatttttta gtagagacaa ggtttcacca ttttgggcag 116700 gctggtctcg aactcccgac ctcaggtgat ctgcccacct cggcctccct aagtgctggg 116760 gttacagaca taagccactg cgcttggcca ggagtttcct ttttaaatca gacccctcaa 116820 tgagaggccc cacagatgca gcctcttgca gacctgccag cccaattctg gagccaggtt 116880 tgttggattc atcctgtatg caaacagctt ctccttaagg ctttcctctg aattcagctc 116940 tggccccacc ctcaaactga cttctaaatg atcccactct tgagcaggcg tctaagagga 117000 atattttcgg gaggtagttg tagttcatgt tactgctgaa ggccacccac ctcacctccc 117060 ctccatacac tttccgcctg gtaaatacag gatatcctgt ccagggcaag aatctgatgt 117120 aagagcctgg attctgcggg gagggccctt ccctctctct ccctcctcct ccctcctggt 117180 gtctgggttg gggaggggtc atggccctga tttggatggc ctgagggtta gcatgagcca 117240 gggtaagtga gacttgttct gggtcaaatc tgggactggc catgacccta aatgaccaat 117300 gcactcctcg cagctctcct gggttgttct gtatctgcta gtcctgagtc cctgggtgga 117360 gggcttccgt tcttgttctc cagacctcat ctcaggccag aacttggaag gaaagacccc 117420 agcatgccct cagttctcgt attcagtgga gtgtgggggc ttgaggacat gaaaaagggc 117480 gtaagtggca gtcccatccc ccttccccat ggaccctaac tcttgttaat atacagaatt 117540 cccatcattc ctggcaggga tcaagacaga cccagattgt cccagaacag cacccacacc 117600 tccctcttca tgctcttcag agagcgcaga gaagtctttt ctcctgacgc tccctccttt 117660 tccctgccct tcccttgacc ccacttgcta agctggagag aaaggttctg ttatctttgt 117720 cccctttccc tcctgcacag aggctctcgt gggggtgggg gggaagcctt ttactgctgc 117780 gtaggcctct gtagcccttc ttgtctgttg cccctcctgc accatctctg agtgaagatg 117840 ttttctgggc tcccagtgct ggctcaaaca cacttctccc gaggtgacca caccctgctg 117900 taagcgctca gagaactttg tctgcacttt ggtatggccc tgaccacaca gtgccgtctt 117960 cttttggttg tgtgacttcc ttgctgctat tatattatta ttattattat tgttagctaa 118020 cattattaag tgcttattat gtgccagaca ttgtgctaaa attttttttt tccatttgga 118080 aaaactgccc taattgacag ataagaaaac tggagctgga aaagtggagc tcaaaaagat 118140 taagtaattt ttatgcatcc gaagtcacac agtcagtaaa cagttgagac cgcttttgta 118200 accacagcag tttgatcttt tccacaatac ttcatgctgc cctaactgta agcttcttgc 118260 attcagggat cttacacaat agtgacatgt aagatctgta agaagatgat aaggatagta 118320 tctgcctcaa agaactgatg taagggttaa ttaagcatta tatataaagc acttgaaatc 118380 gggctcggcc ctcagtcagc actcagtaaa ggtgagttgt tattgttgtt gatgatgatg 118440 ttattattat tattaccatg actattgctg cttctcctgc tacttcattt ggaagaaggt 118500 ggccttgtac ctagggggaa atcagtaaat agcctgtggg tgaatgaatg agtgactgaa 118560 tgatactctt ctgttcttca aggcaggaga ccgggtgatg gtgttgaacc ggtcagggat 118620 gtggcaggaa gaggtgactg tgccctcggt ccagaccttc ctgattcctg aggccatgac 118680 ctttgaggaa gctgctgcct tgctcgtcaa ttacattaca gcctacatgg tcctctttga 118740 cttcggcaac ctacagcctg gccacagcgt cttggtacac atggctgcag gtgacaggtc 118800 ccctcacttt atcacccctt accccaccca gatttccttc caggcccctt ccctgcagcc 118860 tgtctgggtt gttgtcatgg caacaccagg ctgccttggc ctgtggctcc cagaggcctc 118920 tgctgtgtag ttgccgtggt aacattcagg caccaggtct agtctggtgt gctatcctta 118980 gcaacgtgcc ctcaccccac acccccacct ctctagctac cttccccacc acttctcagt 119040 catggaaatt agacacggcc ctaaaatgag cgtaggcaaa atgaaggtga caggctgagt 119100 ccctgggagg ctagaatgga gtggttggtg gccagggcaa ctccatatcc cctgcttatg 119160 ggtgtcttgc tgcagggggt gtgggtatgg ctgccgtgca gctgtgccgt acagtggaga 119220 atgtgacagt gttcggaacg gcctcggcca gcaagcacga ggcactgaag gagaatgggg 119280 tcacacatcc catcgactat cacacgactg actacgtgga tgagatcaag aagatttccc 119340 ctaaaggtgg ggggcataat atgggagggg gtagggaggc acaggacagg gaggggagct 119400 ccagatctgt ggatcctaat gttgttcttg ggttccccta ctctatgaca ggagtggaca 119460 ttgtcatgga ccctctgggt gggtcagata ctgccaaggg ctacaacctc ctgaaaccca 119520 tgggcaaagt cgtcacctat ggtgagttag tgggccaggg atggagagag catgtgaggg 119580 caggagggag ggtctaaggg gtgggatata gaggccaggg cttttgaatg aagaaggggt 119640 agggactcag gtgctctgta gacgatcagg gttaggaatg gtcctgtatg ctgcattcag 119700 attgctgact cttgggtacc agctcttttc attctctgtc acaacttttc atatgagtga 119760 tagtaaattc tacattcttt tttttggttt tttttttgag atggagtttc gctcttgtcg 119820 cccaggctgg agtgcaatgg catgatctcg gtcagtgcaa cctctgcctc ctgggttcaa 119880 gcgattctcc tgcctcaccc tcccgagtag ctggaattac aggtgtctgc caccacgccc 119940 aactaatttt tgtattttta gtagaggcgg tgtttcacca tgttggccag gctggtcttg 120000 aactcctgat ctcaggtgat ccagccgcct cagcctccca aagtgctggg attatagccg 120060 tgagccacca cgcctggcca aattctacat tcttgtttgg ggattattct tgaacaacca 120120 gcctgccttc tttctgtcct acctccctga gcatcttagg cagggtgcat tttcatttaa 120180 aaaagtattt catacaacaa aataagccag gcatggtggc tcatgcctgt aatcccagca 120240 ctttggaagg ccagggcagg cagatggctt gagcctagaa attcgagacc agcctggtca 120300 acatggtgta ccttatctcc acaaaaaata caaaaattag ccaggtgtgg tggcactgta 120360 ctccagcctg ggcaacagag cgagaccctg actcaaacaa atgaacaaac aagcaaatac 120420 ataaagatta gagcaatttt tttttttttg agacagaata tcactctgtt acccatcctg 120480 gagtgcagtg gcgcaacctc ggctctctgc agcatccacc tccctggttc aagcagttct 120540 gcctcaggct cctgagtagc tggaattaca ggtgcccatc tccacgcctg gctttttttt 120600 ttttcttttt cttgagacag agtctggctg tcacccaggc tggagtgcag tgacacgatc 120660 tcggctcact gcaacctcca cctcccggat tcaagcaatt cttctgcctc agcctcccaa 120720 gtagctggga ctgcgggcgc acgccaccat acctggctaa tttttgtatt gttgtgggtt 120780 tttttgtttg ttttgttttg tttttttttt ttgagacgga gtttcgctct ttttgcccag 120840 gctgaagtgc agtggcgcga tctcggctca ctgcaacctc cgcctcccgg gttcaagcga 120900 ttctcctgcc tcagacttcc tgagtagctg ggattacagg catgtaccac catgcccagc 120960 taattttgta ttttcagtag agacggggtt tctccatgtt ggtcacgctg gtctcgaact 121020 cctgacgtcc agtgatccgc ccacctcggc ctcccaaagt gctgggatta taggcgtgag 121080 ccaccatacc cggccaacac ctggctaatt ttcgtatttt ttagtagaga caaggtttca 121140 ccattttggg caggctggtc tcgaactcct gacctcaagt gatcccccca ccttggcttc 121200 ccagagtgct gggattatgg atgtgagcca tagcacccag cccctagagc aatttaaagt 121260 cagccagggt tggtttgggc ctggtaacca gcagtttgag aattatccaa tcactccctg 121320 gcactggtgt ggagaattgc aaggggatca cagggaacag agagcacaga tgcagacaca 121380 cagggatgtg cctggggggg ttcacaggct atgtcacctt gtccttcagg aatggccaac 121440 ctgctgacgg gccccaaacg gaacctgatg gccctggccc ggacatggtg gaatcagttc 121500 agcgtgacag ctctgcagct gctgcaggcc aaccgggctg tgtgtggctt ccacctgggc 121560 tacctggatg gtgaggtgga gctggtcagt ggtgtggtgg cccgcctcct ggctctgtac 121620 aaccagggcc acatcaagcc ccacattgac tcagtctggc ccttcgagaa ggtgaatgtg 121680 aggactttgc agggagggct tgggtaggac tcatgaaggc tggggtccca aggggcagat 121740 tcctggggaa gaggagggct gcctgcatca cactggcccc tgttggatga gggttggata 121800 gcactgggag ccgcatcttt ccttcctccc caggtggctg atgccatgaa acagatgcag 121860 gagaagaaga atgtgggcaa ggtcctcctg gttccagggc cagagaagca gaactagggc 121920 aagtggctgt gagaccctag agaccagcga agggagaagt tgggaagcta cgttctgttg 121980 gccaccagac ttgcatttca gcctctgtca taatgctctg ccctccctcc cccgaagttc 122040 tctgtggtga tgaccgctct cccctgcccc tccccgcttc ctgacctctg aagaggttgg 122100 gaagtgacca tttggatgtc tgggccctgc caaggcgaca gggagggtca gagggaggcc 122160 ggctgcttcc tgcccccacc ctttccccgg gcctgctgtg ctgcttttgt gccaaggtta 122220 gccagtcccc cctgttgtgt tccatgtgct ttcacctctg cctcatcttt cctcccgtcc 122280 ctgccccgcc acctccccaa agaattgaaa cgtcagctca ggatatgggg ccaatctctg 122340 tgagtccagc atgtacctgt ctctccctag tgtcccttca gcctgggctg accagtgccc 122400 gcctctgggc ttgaccagtt cccaatctcg tcctctgtcc ccaacttctt aagcacaatt 122460 gggcttcttc catctccagg ttttctgcca ttcttaacca aggctgcctc ttccaacagg 122520 gcgggaatca gacctactcc cctaggtcac aactctggga aggatacaga gcccccaccc 122580 ttcactgagt tctctggatt tgttctcagt gccttagcaa cgaaaacctg tgcttgtgtg 122640 tgtgtggcgg cggggaggga ggatcctgtt tcccacctcc ttctcctccc ctgtactccc 122700 cagtgccttc cttgttctgg tggagctggg gtttctctcc tccccagtcc cacaacactg 122760 ccaaaaatct gtgtatgtgc cattgggtgg ggcagcccca agcctcctgg ggaggcaggg 122820 caaaaacagg tgccctcatc gtggtctgtg ccatgtcccg tctctatggt ggttgaggag 122880 aaaggcgggg aagcttcctc agccttgcag atatgtgtgg catttactag ccagagctct 122940 gaaaggcagt gctgtctgtt tcttgtactg ggaccaaagt aaaaatccaa gcacattccc 123000 cttgcagtta ggggaggccc tactgccttc tcaaagcaga gaggcagctt atcaaactca 123060 gcccaaaact ctgtttacat gggtggggag atggagcagg gaagtacaga gtgggatggt 123120 caggacctgg gccattgcaa ccaaaatggg gacttcctgg gtagggaggt cactccctct 123180 actcactgag ctaggattag ggagggttat tgccccaacc attgcaatgg gaggtggagg 123240 gacaggctca gcctcctcat tgtctaaatg aggcctaaat gtgtgaagtg cgatttctgc 123300 ttttgtgtac cccaccaccc cattaccaca gctgcctttg tgtgtttgtg tcaataaaaa 123360 gccaaaccct gggtcctgct tgttgcctct gagagtggag ggaaggtgag ctcctggaag 123420 gctagtgctg ccagcagaag atctgggctg cttcctgccc cctgcctctt tccatgccca 123480 aatcacgttt cctttcatga gtgaaatgag gaagaacatc atggcatgca ggctcttttt 123540 actgttctgg gcagtgtttt gcaatgtgtg acccctccgc actgttggtg aacatacaga 123600 cctcctatat gggcacccaa gcccaggcca gtgtgagaac cttggcgggg gggtggggag 123660 gatgagaagg ggaggcccct agcctgactc agaggtgaag actgctaggc cctgctgtcc 123720 ttggggtacg actgtcaggg cctctacctc cccgcccccg cgggtgggct tctggaagtg 123780 gatctccagg acgtcatgca gctccgggcc atccaagata tcaggaatgt tgagcaccag 123840 taccgagcgg ggaactggct gcgacctgat ctggaaaagg agccaggaga tggcaaaggc 123900 tcatgggaga agggctgggg gctgggggta gggcaggcag tgccccatgg gggtatgagg 123960 tcgggaggcc tggagaggct gatggtgggt aggtaggtca gtggggtttg gggcctctga 124020 tccttcattg ggcaagttcc tggcaggcag acaggttacc cagcccagcc cctgttcttc 124080 acccctcctg cttacctcag ccttctggat ctccccattc acatacggag agactctcag 124140 agggacttgc tgcccaccca gtggcactgt gaactggccg atttggcaca gacgctgagc 124200 cactgtgggg agcaaggagg ggtgggcctt tagcatcaag ccctctcctc tccctgcacc 124260 ataatcttgc acaccctata ccctctcccc tgcaggaggc ctgcatagcc ctcacctcca 124320 tccctagcaa accccagcat gacactccct ggcagtagct cccgaacgtc cacatcgcca 124380 cctccgttcc tagtcttgcc aaagaagatc tctagcttgt ccagcagctc ctcctcactc 124440 agcctgaggc tggcaggaaa tccagtgacc aacaccctcc ggccactcaa ctggctggac 124500 acctaggggg agacagcaag gggtggtccc agacacagct ccacttcccc atgcccaggt 124560 gcatggcatg ctttgcatgc cccaggattc tgtcatacca tcacctggat ggtggtgacc 124620 atgggcagct ccaagggctg gacctgcacc cgcagccggc actcctccat gttgatcgtg 124680 tgctcctttt gttgcagcac ctgctcagcc actgggtggt gggaaacagg gtcagtactg 124740 ggaaccctcc ccacctccct cctgaggctc cccatgagct tacctttggg gtcatcaaag 124800 gtgatcagag cagagcccgc aagcagaggg cagtggatcc gcaaattgga aactaaagac 124860 ttaggcactt ccgggtcctg ctgggtgtgt cctcggaata ccagggggat cttgggcact 124920 gaaaatggga cctggaagta ggggagggga gtaggagtgt tcctcactcc cacctaggag 124980 gaaggcatct ccgattccat tccattgatg ctgagtgccg gagataaata catttactga 125040 aagaaaagct ggataaatga gtggatgaat gcaggtctgg tccatacagg gcaatttaca 125100 tacaacatct taatttgtcc tgggaggtgg gtagctctac tttacagatg ttcaagtaac 125160 ataatggagg tcacacagca aggaagtagc agagccagga ataaaaccga gaactcccca 125220 gctctttttt gtgtttcttt gttttaaagg gagtcttgct ctgtcaccca gctggagtgt 125280 agtggcatga tcttggctca ctgcaacctc cacttcccag gttcaagcaa ttcggactca 125340 gcctcccaag tagctgggat tacaggcatg tgccaccaaa cccagctaat ttttgtattt 125400 ttagtagaga cggggtttca ccctgttggc caggctggtc tcaaactgac ctcaggtgat 125460 ccaccagcct cggcctccca aagtgctggg attacaggcg tgagccactg cgcccggcct 125520 aatttttgta tttttagtag agatgggatt tcactgtgtt ggccaggctg gtctcaaact 125580 cctgacctga ggtgatcagg cccccttggc ctaccaaagt gctgggttta caggtgtgag 125640 ccaccgcacc cggcctcgcc agctcgtttt taccaaacaa caccagatcc tttagggggg 125700 gttattgcgg gcggattttt gaaacggagg gctggtgata ggctttttat aggtatgcat 125760 gtatatggtt ctagcgtagt ggattttggg aattgcggtg ggtatctaag atagatatcc 125820 tgtgatcctt attttattga tttatttttt taatttttat ttatttattt atttttgaga 125880 cagagtcttg ctctgtctcc caggctgggg tgcagtggcg cgatcttggc tcactgcagc 125940 ctccacctcc caggatcaag taattctcct gcctcagcct cccaagtagc tgggattaca 126000 ggcacccacc accacacctg gctcattttt gtatttttag tagaaacagg ttttcaccat 126060 gttggccagg ttggtctcaa actcctgacc tcagatgatc tgcccgcctc ggcctcctaa 126120 agtgctagga ttacaggtgt aagccacaat gcctggccaa tccttatttt atagatgagg 126180 aaattaaagc tcagagaggt taaatgactt gcccaaagtc atttggccct aggctgtctg 126240 actccagagc ccacccacta acctgtgctt tacagtgaag aaatgaagcc cagagtgggg 126300 aggtagttta cccatcaatt ctagcttgtc cctggactgt cacactttcc actgtacacc 126360 aagtaacctt ttaggctggg tgtgatctgg aatgggtcca gagagagaac tgacatcaca 126420 ggcagggaag tgacaccagg gataccaata aatgcacctt tgtttgtgga atagagcaga 126480 gttcaccctg tggttaggaa tcctgataaa gaagttcagc tcagagaagc atgagatctc 126540 ttggaaagat aggactctgt tctgaccatc tctgtattcc ttgtgtccag caagatctcc 126600 ggcacaaaat atgtgtccgg taaaactgtg ttgaatgaag aaatgaagtg aatgaatgac 126660 ggtaaaggag cacattacag aggacaccaa agaaattcag tgtgagtttg ttctattttt 126720 agcagaagaa tactagagct tgaccaaatt atgctggttt atgaatagtg aaaaagatca 126780 ttagttattc atatttctgt aactcagaga gtgctaacac agtgccttta agggccagtt 126840 ggatgacatt aatgagttaa tagagccatg taggataaca gagagtggtg gggactctga 126900 cgcactggga agagcatgtc ctttctaaag taaactgctt ctagccataa caaagtttcc 126960 ccccacagca aatctaccca tgtttttgtt ttgttttgtt ttttgagaca aagtctcaat 127020 gccacccagg ctggagtgca attgctccat tatggctcac tgcagcctcg acctcctgga 127080 atcaatcaat cctctcatct cagcctcctg agtacaggcg tgtgccatca tgccagctat 127140 tttttttttt tcttcttttt gggacggagt ctcaccctgt cgcccaggct ggagtgcagt 127200 ggcgcgatct ctgctcactg caagcttcgc ctcccagttc acttcattct cctgcctcag 127260 cctcccgatt agctgggact acaggtgccc gccaccacgc ctggctaatt tttttgtatt 127320 tttagtagag acggggtttc accgtgttag ccaggatggt ctcgatctcc tgacttcatg 127380 atctgcccgt cttagcctcc caaagtgctg ggattacagg tgtgagacac cgcgcccagc 127440 cctctatttt tttttctttt ctgagacgga gtctccctct gttgcctagg ctggagtgca 127500 gtggcgcaat atcggctcgc tgcaaactcc acctcccgga ttcaacagat tctcctgcct 127560 cagcctccca agtagctggg attacaggca cctgccacca ctcctggcta atttttttta 127620 ttttttattt atttatttat tttgagacag agtctcgctc tgtcgccagg ctggaatgca 127680 gtggcaggat ctcggctcac tgcgacctct gactcccggg ttcaagcgat tctcctgcct 127740 cagcctcccg agtagctggg actacaggca cgcaccacca tgcccagcta atttttgtat 127800 ttttagtaga gatggggttt caccatgttg gccaggatgg tctcaatctc ttgacctcgt 127860 gatccaccca cctcggcctc ccaaagtgct gggattacag gagtgagcca ccgtgcccgg 127920 ctctaatttt ttatttttag tagagatggg gtttcaccat gttggccagg ctggtctcaa 127980 acttcccacc tgaagtgatc tgcccaactc agcctcacaa agtgctggga ttacaggcag 128040 gagccacgga cccaggcccc ctaatcttcc catttttaat agaaataaaa aatctgggca 128100 ggttgttgtg gcacatgcct gtaatcccag cactttggga ggccaaggga ggcagatcgc 128160 ttgagcccag gagtctgaga ccagcctggg caacaggaca aaactctacc tctacaaaat 128220 atttaaaaat tagccaggca tggtggcaca tgcctgtagt cccagctact cgggaggctg 128280 agatggaagg atctattgat ccctagaggt ggaggtggct gcagtgagcc atgatccagc 128340 cactgcactg cagcctggaa aaaacagtga gatcttgtct ccaaaaaaca aaaaatctgg 128400 atttttattt gaaaaagatg gcccaattta acgtatataa agccgggtgc tgtggctcaa 128460 gcctgtaatc tcagcatttt gggaggctaa gggaggcaga tcatgtgagg tcaggagttc 128520 gagaccagcc tggccaacat gctgaaaccc tgtctctaca aaaaattagc catgctgggc 128580 acggtggctc acgcctgtaa tcccagcact ttgggaggct gaggcaggcg gatcacgagg 128640 tcaggagttc gagaccatcc tgcctaacac agtgcaaccc catctctacc aaaaatacaa 128700 aaaactagct gggcgtggtg gcgggtgcct gtagtcccag ctacttggga ggctgaagca 128760 agagaatggc atgaacccat ggggcggagc ttgctgtgag ccgagatcct gccactgcac 128820 tccagcctgg gtgacagagc gagactccat ctcaaaaaaa aaaaaaaaaa aaaaaaatga 128880 gccaggcgtg gtggcatgtg tgcctataat cccagctact tgggatgctg aggcaagaga 128940 atcacttgaa tctggaaggc agaggttgca gtgagccaag atcatgctat tgcacttcag 129000 cctgggcaac aagagtgaaa ctccatctca aaaaaaaaaa aaaaaaaaaa aggaaagaaa 129060 agtccgggca tggtggctta cacctgtaat cccagcactt tgggagcttg aggggggcag 129120 atcacgaggt cagaagatca agaccatccc ggctaacacg gtgaaactcc atttctacta 129180 aaaatacaaa aaattagcca ggcatggtgg aacgtgcctg tactcccagt tacttgggag 129240 gctgaggcag gagaatcgct tgaacccggg aggcagaggt tgcagtgagc cgagatcatg 129300 ccactgtact ccagcctagg agacagagtg agactccgtc tcaaaaaaaa aaaaaaaaaa 129360 gggattgtcc ttggggaact ggggttctga aaaggttggc aataataata ttaagaagaa 129420 acacatattg aatgctctgt aggtgctaag cagtgggata agtttttacc gtgttaatct 129480 atggattacc tagtgtgatt cttaaagtat aattcttata gtatatatat atatatatat 129540 atatataaat tttgtgtgtg tgtgtgtgtg agagacagtc tccctctgtt gcccagagtg 129600 gagcatagtg gtacaatctc ggctcactgc aacctctgcc tcccaggttc aagcaattct 129660 cccgcctcag tctccctagt agctgggatt acaggtgtgt gccaccatgc ctggctaatt 129720 tttgtgtttt tagtagagat ggggttttgc tatgttggcc aggctggtct cgaactccta 129780 acctcaagtg atccacacgc ctcagcctcc caaagtgctg gctgggatta caggtgtgag 129840 ccaacacacc cagcctaatt cctttagttt aatttttttt tttttttttt tagacagagt 129900 ctcgctgtgt cacccaggct ggagtgcagt gatgcaatct cggctcactg caacctccgc 129960 ctcccaggtt caagtgattc tcctgtctca gcctcccaag t 130001 24 20 DNA Artificial Sequence Antisense Oligonucleotide 24 actggcttat ctttctgacc 20 25 20 DNA Artificial Sequence Antisense Oligonucleotide 25 ggactctaat ttcttggccc 20 26 20 DNA Artificial Sequence Antisense Oligonucleotide 26 agataaatcc atttctttct 20 27 20 DNA Artificial Sequence Antisense Oligonucleotide 27 ccctgaagat ctttctgtcc 20 28 20 DNA Artificial Sequence Antisense Oligonucleotide 28 tacataaaat atttagtagc 20 29 20 DNA Artificial Sequence Antisense Oligonucleotide 29 gggaaaccag ctattctctt 20 30 20 DNA Artificial Sequence Antisense Oligonucleotide 30 gtagctggga ttacaggtgt 20 31 20 DNA Artificial Sequence Antisense Oligonucleotide 31 ccagaggtct tatattttaa 20 32 20 DNA Artificial Sequence Antisense Oligonucleotide 32 tcatgccaga ggtcttatat 20 33 20 DNA Artificial Sequence Antisense Oligonucleotide 33 tggtgggatc tgtcatttta 20 34 20 DNA Artificial Sequence Antisense Oligonucleotide 34 actttttctt ccttcagcaa 20 35 20 DNA Artificial Sequence Antisense Oligonucleotide 35 accaagttta tttgcagtgt 20 36 20 DNA Artificial Sequence Antisense Oligonucleotide 36 attcccccac ggacactcag 20 37 20 DNA Artificial Sequence Antisense Oligonucleotide 37 acgcccggct aatttttgta 20 38 20 DNA Artificial Sequence Antisense Oligonucleotide 38 ctctgtcgcc caggctggag 20 39 20 DNA Artificial Sequence Antisense Oligonucleotide 39 ttccaatgaa cagccggtgt 20 40 20 DNA Artificial Sequence Antisense Oligonucleotide 40 ttccaatgaa ccagagcaga 20 41 20 DNA Artificial Sequence Antisense Oligonucleotide 41 tcacaagcag ctttacccag 20 42 20 DNA Artificial Sequence Antisense Oligonucleotide 42 gctgcttcac ccaattcaat 20 43 20 DNA Artificial Sequence Antisense Oligonucleotide 43 aactcagcat ctttttctga 20 44 20 DNA Artificial Sequence Antisense Oligonucleotide 44 tgggtcaccc ctttttctga 20 45 20 DNA Artificial Sequence Antisense Oligonucleotide 45 aactcagcat ctttccactc 20 46 20 DNA Artificial Sequence Antisense Oligonucleotide 46 tcacaagcag ccaattcaat 20 47 20 DNA Artificial Sequence Antisense Oligonucleotide 47 gatgctgctt cacccttttt 20 48 20 DNA Artificial Sequence Antisense Oligonucleotide 48 gctgcttcac cctgatactt 20 49 20 DNA Artificial Sequence Antisense Oligonucleotide 49 tcccatgctg ttctaacaca 20 50 20 DNA Artificial Sequence Antisense Oligonucleotide 50 gagtaagacc ttgcaaaata 20 51 20 DNA Artificial Sequence Antisense Oligonucleotide 51 catgcaaaat agtcccagct 20 52 20 DNA Artificial Sequence Antisense Oligonucleotide 52 actctactac ctttacccag 20 53 20 DNA Artificial Sequence Antisense Oligonucleotide 53 tcatacatac cagccggtgt 20 54 20 DNA Artificial Sequence Antisense Oligonucleotide 54 gagtaagacc ctgtctcaaa 20 55 20 DNA Artificial Sequence Antisense Oligonucleotide 55 gtgcacttac agtcccagct 20 56 20 DNA Artificial Sequence Antisense Oligonucleotide 56 acagaactac cctgatactt 20 57 20 DNA Artificial Sequence Antisense Oligonucleotide 57 gttaatactg ctttaaatgg 20 58 20 DNA Artificial Sequence Antisense Oligonucleotide 58 ttctccccag gcagccaagt 20 59 20 DNA Artificial Sequence Antisense Oligonucleotide 59 aggctcttac ctgtgggcat 20 60 20 DNA Artificial Sequence Antisense Oligonucleotide 60 tctgtctgac tgaacgaagg 20 61 20 DNA H. sapiens 61 ggtcagaaag ataagccagt 20 62 20 DNA H. sapiens 62 gggccaagaa attagagtcc 20 63 20 DNA H. sapiens 63 agaaagaaat ggatttatct 20 64 20 DNA H. sapiens 64 ggacagaaag atcttcaggg 20 65 20 DNA H. sapiens 65 aagagaatag ctggtttccc 20 66 20 DNA H. sapiens 66 acacctgtaa tcccagctac 20 67 20 DNA H. sapiens 67 ttaaaatata agacctctgg 20 68 20 DNA H. sapiens 68 atataagacc tctggcatga 20 69 20 DNA H. sapiens 69 taaaatgaca gatcccacca 20 70 20 DNA H. sapiens 70 ttgctgaagg aagaaaaagt 20 71 20 DNA H. sapiens 71 acactgcaaa taaacttggt 20 72 20 DNA H. sapiens 72 ctgagtgtcc gtgggggaat 20 73 20 DNA H. sapiens 73 tacaaaaatt agccgggcgt 20 74 20 DNA H. sapiens 74 ctccagcctg ggcgacagag 20 75 20 DNA H. sapiens 75 attgaattgg gtgaagcagc 20 76 20 DNA H. sapiens 76 aaaaagggtg aagcagcatc 20 77 20 DNA H. sapiens 77 aagtatcagg gtgaagcagc 20 78 20 DNA H. sapiens 78 acaccggctg gtatgtatga 20 79 20 DNA H. sapiens 79 tttgagacag ggtcttactc 20 80 20 DNA H. sapiens 80 agctgggact gtaagtgcac 20 81 20 DNA H. sapiens 81 aagtatcagg gtagttctgt 20 82 20 DNA H. sapiens 82 acttggctgc ctggggagaa 20 83 20 DNA H. sapiens 83 atgcccacag gtaagagcct 20 84 20 DNA H. sapiens 84 ccttcgttca gtcagacaga 20 

What is claimed is:
 1. A compound 8 to 80 nucleobases in length targeted to a nucleic acid molecule encoding breast cancer-1, wherein said compound specifically hybridizes with said nucleic acid molecule encoding breast cancer-1 and inhibits the expression of breast cancer-1.
 2. The compound of claim 1 which is an antisense oligonucleotide.
 3. The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified internucleoside linkage.
 4. The compound of claim 3 wherein the modified internucleoside linkage is a phosphorothioate linkage.
 5. The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified sugar moiety.
 6. The compound of claim 5 wherein the modified sugar moiety is a 2′-O-methoxyethyl sugar moiety.
 7. The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified nucleobase.
 8. The compound of claim 7 wherein the modified nucleobase is a 5-methylcytosine.
 9. The compound of claim 2 wherein the antisense oligonucleotide is a chimeric oligonucleotide.
 10. A compound 8 to 80 nucleobases in length which specifically hybridizes with at least an 8-nucleobase portion of a preferred target region on a nucleic acid molecule encoding breast cancer-1.
 11. A composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier or diluent.
 12. The composition of claim 11 further comprising a colloidal dispersion system.
 13. The composition of claim 11 wherein the compound is an antisense oligonucleotide.
 14. A method of inhibiting the expression of breast cancer-1 in cells or tissues comprising contacting said cells or tissues with the compound of claim 1 so that expression of breast cancer-1 is inhibited.
 15. A method of treating an animal having a disease or condition associated with breast cancer-1 comprising administering to said animal a therapeutically or prophylactically effective amount of the compound of claim 1 so that expression of breast cancer-1 is inhibited.
 16. The method of claim 15 wherein the disease or condition is a hyperproliferative disorder.
 17. The method of claim 16 wherein the hyperproliferative disorder is cancer.
 18. The method of claim 17 wherein the cancer is of the breast, ovary, prostate, or peritoneum.
 19. The method of claim 15 wherein the disease or condition results from a chromosomal translocation event.
 20. A method of screening for an antisense compound, the method comprising the steps of: a. contacting a preferred target region of a nucleic acid molecule encoding breast cancer-1 with one or more candidate antisense compounds, said candidate antisense compounds comprising at least an 8-nucleobase portion which is complementary to said preferred target region, and b. selecting for one or more candidate antisense compounds which inhibit the expression of a nucleic acid molecule encoding breast cancer-1. 